Pressure Medical Technology
Chamber Sales Handbook
Welcome to the team!
This website is here to help guide you through the sales process and ensure you have the tools required to dive into HBOT and help heal the world with Oxygen Under Pressure!
Dive Into HBOT
Welcome to the forefront of Hyperbaric Oxygen Therapy sales,
where innovation meets healthcare excellence.
For over 20 years, we've been at the forefront of Hyperbaric Oxygen Therapy, not just offering treatment, but building premier clinics that set the standard for excellence.
Hyperbaric chambers represent a cutting-edge solution in medical technology, offering a noninvasive and scientifically proven method to enhance healing and recovery processes. You are now part of expanding access to this revolutionary treatment. Use this guide to learn more about HBOT, the chamber specifications, our offerings and how to close a sale.
Meet the Team
At Pressure Medical Technology, we bring nearly two decades of unparalleled expertise in Hyperbaric Oxygen Therapy (HBOT) and hyperbaric chamber solutions. With our extensive experience, we have expanded beyond patient care to become the trusted experts in hyperbaric chamber sales, consulting, and regulatory compliance.
Dr. Alexander
Borsand
Co-Owner
Hannah
Stephens
Co-Owner
Tiffany
Boyer
Accounting
Sarina
Gomez
Inside Sales
Lets Start With Getting Paid..
As a sales representative at Pressure Medical Technology, you are classified as a 1099 independent contractor and will be compensated on sales through a simple comission structure.
You will receive 8.0% commission on all sales related to:
- Hyperbaric Chambers
- Accessories
- Training Programs
- Business Plans
- Consulting Services
Once you sell two hyperbaric chambers in a 12 month period, you will be riased to 10% comission. You will retain this comission rate for a period of 12 months as long as you sell an additional chamber.
Here is a quick example of a sales comission:
You sell a clinic two ATAMOX 40 Hyperbaric chambers, two lights and two speakers. They recieve free training, but need to send an additional staff member to our accredited training course (Another sale!). Then while at training they realize that our clinics have figured out how to thrive in HBOT and they decide to purchase our entry level Business Implementation Plan and then sign up for our CRM. Because they are an awesome customer you provided a 3.0% discount ($8,400).
The comission on this sale at 8.0% is $17,472
Benefits - Sales representatives are eligible to receive Hyperbaric Oxygen Therapy (HBOT) as a unique perk of their affiliation with the clinic.
You are eligible for up to three free HBOT treatments prior to making your first sale.
Once you make your first sale, you are entitled to daily HBOT treatments, subject to availability, for the remainder of the year.
Empower - Elevate - Oxygenate - Get Paid
All Of The Details
Chamber Specifications
ATAMOX 40
Hyperbaric Chamber
Made In America - 100% American Steel
The ATAMOX 40 is one of the largest and most versatile monoplace hyperbaric chambers on the market, offering physicians the ability to treat patients at operating pressures up to 4.0 ATA, or 43 psi.
Its generous 40-inch interior diameter provides patients with a more spacious and comfortable treatment experience, while its thoughtful design allows it to fit into most offices and clinical environments.
Built with fully in-house manufactured mirrored controls both inside and outside the chamber, the ATAMOX 40 is engineered for safety, reliability, and flexibility across a wide range of hyperbaric protocols.
Key Points
FDA Cleared, ASME, PVHO 4.0 ATA Chamber
Allows for Self Treatment
Almost Maintinance Free
Perfect Safety Record for Over 20 Years
A new standard in hyperbaric chamber safety, comfort, and performance.
Built by a manufacturer recognized for exceptional safety standards and reliable, low-maintenance design, this chamber was created to elevate the patient experience.
With a spacious interior and comfort-focused design, patients no longer feel confined or overwhelmed. Instead, they can relax, stretch out, and focus on healing in one of the safest and most comfortable hyperbaric chambers available.
$99,000
Pressure Rating:
Rated to 4.0 ATA, the highest rating on the market.
Competitor chambers are typically rated between 2.0 and 3.0 ATA
Windows are rated to 10 ATA, exceeding regulatory standards
Dimensions:
External: 43 inches (W) x 96 inches (L)
Internal: 40 inches (W) x 88 inches (L)
Internal Volume 70.4 ft3/ 1.99 m3
Weight: 1,250 lbs - the lightest FDA chamber on the market
Pressurization Rate 1 to 6 PSI/min
Purge Rate 280-800 Ipm/ 30 PSI
Flow-Through Design:
Compressed with medical air / air compressor
Most efficient chamber at 1,100 liters of oxygen per treatment
Constant air exchange ensures complete air turnover every 15 minutes, eliminating concerns about CO2 or excess oxygen buildup
Safety:
Recognized as the safest chamber based on incident reports
Every valve is mirrored on the inside for self-treatment and safety redundancies
Certifications:
FDA Cleared (510K) - MAJOR SELLING POINT
Certified by ASME and PVHO - Stamped on leg of chamber with serrial number
Multiplace
Hyperbaric Chambers
100% Customizable for Clinet
Millennium Modular Multiplace Hyperbaric Chambers are custom-designed to meet the needs of each facility, with configurations available for 4 to 12 patients and options for single-lock or double-lock designs.
Each chamber is rated up to 3.0 ATA and can be tailored with custom seating, flooring, and interior layout options to support patient comfort, clinical workflow, and operational efficiency. Built with both primary and secondary fire suppression systems, the Millennium Multiplace Chamber is designed to deliver a safe, reliable, and highly adaptable hyperbaric environment for modern medical facilities.
Key Points:
FDA, ASME, and PVHO-1 Certified
Custom Sizing and Configuration
Tailored seating, flooring, and accessibility
Layout options to support patient comfort
Starting at:
$650,000
Documentation
Certification Proof
Make the Sale With Documentation of Certifications
FDA 510k
What is it?
The FDA 510(k) is a formal clearance issued by the U.S. Food and Drug Administration allowing a medical device to be legally marketed in the United States. To receive a 510(k), the manufacturer must demonstrate that the device is substantially equivalent to an existing legally marketed medical device in terms of safety, performance, and intended use.
Hyperbaric chambers that are intended for medical treatment in the United States must have FDA 510(k) clearance before they can be legally sold for medical use.
Why It Matters
FDA 510(k) clearance is much more than paperwork. It demonstrates that the chamber has undergone a comprehensive regulatory review and meets the standards required for use as a medical device.
A cleared chamber provides confidence that:
The chamber has been evaluated by the FDA.
The device is manufactured under FDA Quality System Regulations (21 CFR Part 820).
Safety, labeling, performance, and intended use have been reviewed.
The chamber can be legally used in a medical practice in the United States.
Patients and providers are using equipment designed specifically for medical applications.
Without FDA clearance, a chamber may not legally be marketed for treating medical conditions, regardless of the manufacturer's marketing claims.
Why Customers Should Care
Purchasing a hyperbaric chamber is a long-term investment.
Choosing a chamber with FDA 510(k) clearance helps protect the facility by providing:
Regulatory compliance
Greater confidence for physicians and medical directors
Improved acceptance by hospitals and healthcare organizations
Stronger documentation for accreditation and inspections
Increased long-term resale value
Many insurance carriers, healthcare systems, and medical professionals expect equipment to carry FDA clearance before incorporating it into patient care.
Talking Points for Sales Representatives
When discussing FDA clearance with a customer:
Explain that FDA 510(k) clearance is required for all hyperbaric chambers marketed in the United States.
Emphasize that this is evidence of regulatory review, not simply a marketing claim.
Help customers understand the difference between medical-grade equipment and Temu knockoff chambers.
If comparing products, encourage customers to ask every manufacturer for a copy of their FDA 510(k) clearance.
If a manufacturer cannot readily provide their FDA clearance documentation, that should prompt additional questions.
Provide This Certificate to Customer
ASME PVHO-1
What is it?
ASME PVHO-1 is the internationally recognized engineering standard for Pressure Vessels for Human Occupancy. Developed by the American Society of Mechanical Engineers (ASME), this standard establishes the design, manufacturing, testing, inspection, and safety requirements for pressure vessels intended to safely contain people under pressure.
Hyperbaric chambers built to the ASME PVHO-1 standard are engineered to meet rigorous mechanical and structural safety requirements before they are placed into service.
Why It Matters
A hyperbaric chamber is a pressure vessel, and patient safety depends on its ability to safely withstand repeated pressurization over many years of operation.
Compliance with ASME PVHO-1 demonstrates that the chamber has been designed and manufactured in accordance with one of the most respected engineering standards in the world.
This includes requirements for:
Structural design and engineering calculations
Material selection and traceability
Weld quality and inspection
Pressure testing and safety verification
Documentation and quality assurance throughout manufacturing
These standards help ensure the chamber is built to safely withstand the demanding conditions of routine clinical use.
Why Customers Should Care
Purchasing an ASME PVHO-1 compliant chamber provides confidence that the equipment has been engineered with long-term safety and reliability in mind.
Facilities benefit from:
Industry-recognized engineering standards
Enhanced patient and operator safety
Greater confidence from physicians and medical directors
Support for accreditation and regulatory compliance
Increased long-term value and serviceability
Many hospitals, healthcare organizations, and experienced hyperbaric programs consider ASME PVHO-1 compliance an essential requirement when selecting a hyperbaric chamber.
Talking Points for Sales Representatives
When discussing ASME PVHO-1 with a customer:
Explain that ASME PVHO-1 is the gold standard for pressure vessels designed for human occupancy.
Emphasize that the standard focuses on engineering integrity, structural safety, and manufacturing quality.
Encourage customers to ask every manufacturer whether their chamber is built and certified to ASME PVHO-1 standards.
Remind customers that not every chamber on the market meets this internationally recognized standard.
Remind a customer that being built to the standard means nothing without the certifications.
Provide This Certificate to Customer
GR-1 Manufacturer's Data Report
What is it?
The ASME GR-1 Manufacturer's Data Report is an official document completed during the manufacturing of an ASME PVHO-1 pressure vessel. It records key information about the chamber, including the manufacturer, serial number, materials, pressure ratings, inspections, and testing performed during production.
Each GR-1 form is unique to the individual chamber and serves as its permanent manufacturing record.
Why It Matters
The GR-1 provides documented proof that the chamber was manufactured in accordance with the applicable ASME PVHO-1 requirements and that all required inspections and testing were completed.
It also establishes traceability throughout the life of the chamber, making it an important document for service, inspections, repairs, and future ownership.
Why Customers Should Care
Receiving the GR-1 with a chamber provides confidence that the pressure vessel has a complete manufacturing history and documented quality assurance.
Benefits include:
Permanent manufacturing documentation
Verification of inspections and testing
Easier service and maintenance records
Greater confidence during resale or ownership transfer
Added documentation for regulatory and accreditation purposes
Talking Points for Sales Representatives
Every ASME-manufactured pressure vessel should have a corresponding GR-1 Manufacturer's Data Report.
The GR-1 acts as the chamber's "birth certificate," documenting how and when it was built.
Customers should expect this documentation as part of purchasing a medical-grade hyperbaric chamber.
Explain that this is a sample GR-1 and they will be provided with their unique GR-1 with their chamber seial number at time of purchase.
Make sure they are asking competitors for the same documents, as we are providing more paperwork than any other chamber distributor, we are proving what we claim.
Chambers from Turkey may provide fake documents, so our set us apart.
Provide This Certificate to Customer
Acrylic Window Certification
What is it?
Every Hyperbaric for Life chamber includes certified acrylic viewing windows manufactured and tested specifically for use in human-occupied pressure vessels. Our windows are individually certified and rated to withstand pressures up to 10.0 ATA, far exceeding the maximum operating pressure of the chamber and well beyond regulatory requirements.
Our acrylic windows are also among the thickest in the industry, providing an exceptional margin of safety and long-term durability.
Why It Matters
The viewing windows are one of the most critical safety components of any hyperbaric chamber. Thicker acrylic experiences less stress during each pressurization cycle, helping reduce material fatigue and extending the service life of the window.
Because of their increased thickness and 10.0 ATA rating, our windows require less frequent maintenance and replacement than many thinner designs, allowing chamber longevity to be measured in years rather than treatment cycles.
ASME PVHO-1 provides guidance for acrylic replacement at 20 years, supporting long-term ownership and predictable maintenance planning.
Why Customers Should Care
Certified acrylic windows provide confidence that one of the chamber's most important pressure boundaries has been independently tested and documented.
Benefits include:
Individually certified acrylic windows
Rated to 10.0 ATA for an exceptional safety margin
One of the thickest acrylic window designs in the industry
Reduced long-term maintenance and replacement costs
Long service life supported by ASME PVHO-1 guidance
Talking Points for Sales Representatives
Our windows are certified to 10.0 ATA, more than three times our maximum operating pressure.
Thicker acrylic means lower stress during every treatment, contributing to longer service life.
Unlike some chambers that track window life by treatment count, our design is intended for long-term ownership, with ASME PVHO-1 providing a 20-year replacement guideline under normal use.
Acrylic chambers require recondtioning within 10 years.
Provide This Certificate to Customer
Chamber Valve Certification
What is it?
Our chamber valves are proudly designed and manufactured in the USA by an aerospace engineer specifically for Hyperbaric for Life chambers. Unlike off-the-shelf industrial valves, these components were engineered exclusively for hyperbaric medicine, emphasizing precision, reliability, and long-term serviceability.
Each valve is supplied with a Certificate of Compliance, verifying that it meets the required manufacturing and quality standards.
Why It Matters
The valves are among the most frequently used components on a hyperbaric chamber, controlling pressurization, depressurization, and patient safety during every treatment.
Because they were designed specifically for this chamber, the valves feature replaceable internal components, allowing routine maintenance and repairs without replacing the entire valve assembly. This reduces downtime, lowers long-term ownership costs, and helps keep the chamber operating for years to come.
Why Customers Should Care
Purpose-built valves provide confidence that every treatment is supported by components designed specifically for hyperbaric use.
Benefits include:
Designed and manufactured in the USA
Engineered specifically for Hyperbaric for Life chambers
Replaceable internal components for simplified maintenance
Lower long-term service costs
Certificate of Compliance included with every valve
Talking Points for Sales Representatives
These are not generic industrial valves. They were designed specifically for hyperbaric medicine by an aerospace engineer.
The valves are fully serviceable with replaceable internal parts, helping reduce maintenance costs over the life of the chamber.
Every valve includes a Certificate of Compliance for complete quality documentation.
Explain these are not off the shelf parts and supply chain will never be an issue.
Provide This Certificate to Customer
Mattress Material Certification
What is it?
Our chamber mattresses are manufactured using medical-grade antimicrobial vinyl designed for clinical environments. The materials are selected to support patient comfort while also meeting important safety, cleaning, and fire protection requirements for hyperbaric chamber use.
The mattress material documentation verifies compliance with applicable standards, including NFPA 99 smolder rate expectations and California fire protection ratings.
Why It Matters
In hyperbaric medicine, every material placed inside the chamber matters. Mattresses must be easy to clean, resistant to microbial growth, and appropriate for use in an oxygen-enriched clinical environment.
Using certified medical-grade materials helps reduce infection-control concerns, supports facility safety protocols, and demonstrates that the chamber interior was designed with hyperbaric safety in mind.
Why Customers Should Care
Certified mattress materials help facilities maintain a safer, cleaner, and more compliant treatment environment.
Benefits include:
Medical-grade antimicrobial vinyl
Documentation supporting NFPA 99 smolder rate compliance
Meets California fire protection ratings
Supports infection-control protocols
Designed for repeated clinical use
Talking Points for Sales Representatives
The mattress is not a standard consumer cushion. It uses medical-grade antimicrobial vinyl selected for clinical and hyperbaric safety.
Material documentation helps support NFPA 99 compliance and fire safety review.
These details matter during inspections, accreditation, and long-term facility safety planning.
Has the competitor even addressed this vital issue of fire protection?
Provide This Certificate to Customer
Medical Air Compressor Certification
What is it?
Our medical air compressor is specifically designed for hyperbaric medicine and is UL certified as a medical device. The system delivers Grade D clean, breathable air through a multi-stage filtration system, ensuring a safe and reliable air supply for every treatment.
Powered by a double-headed, oil-less ½ HP compressor with an integrated cooling radiator, the system also features a high-efficiency inline filtration system capable of filtering particles down to 0.01 microns.
Why It Matters
The compressor is the heart of every hyperbaric chamber. Patients breathe compressed air throughout treatment, making air quality, reliability, and filtration essential to both safety and performance.
An oil-less design eliminates the risk of oil contamination, while the Grade D breathing air standard and 0.01-micron filtration provide exceptionally clean air suitable for medical applications.
Why Customers Should Care
A certified medical air compressor provides confidence that the chamber is supplied with clean, dependable breathing air designed specifically for patient care.
Benefits include:
UL certified medical device
Supplies Grade D clean, breathable air
Oil-less compressor design eliminates oil contamination
High-efficiency filtration to 0.01 microns
Engineered for reliable, continuous clinical operation
Talking Points for Sales Representatives
Our compressor is built specifically for medical hyperbaric applications, not adapted from an industrial air compressor.
The oil-less design and multi-stage filtration help ensure exceptionally clean breathing air for every treatment.
Every compressor includes documentation verifying its medical certification and air quality standards.
All the parts
Know Your Chambers
Pressure Relief Valves
The Flow-Through Air Valves automatically regulate chamber pressure by allowing compressed air to exit the chamber at a preset pressure.
Available in fixed settings from 1.3 ATA to 3.0 ATA, these valves provide smooth, consistent pressure control while enhancing patient safety and reducing operator workload.
Each chamber includes five customer-selected valves, with additional preset valves available for purchase at any pressure to support different treatment protocols and clinical applications.
Vent Valve
The Vent Valve is used during the final stage of decompression to safely release the remaining air pressure from the chamber, allowing the door to be opened more quickly once atmospheric pressure is reached.
It also serves as an important safety feature by allowing the operator to rapidly vent excess oxygen from the chamber should oxygen concentrations approach unsafe levels, helping maintain a safe treatment environment.
The vent filters air leaving the chamber and the filtration element can be replaced as needed.
Control Panel Console
The Control Panel is the operator's primary interface for monitoring and controlling every treatment. It houses the Air Inlet and Air Outlet control valves, Flow-Through System controls and pressure gauge, oxygen inlet and oxygen flow meter, chamber pressure gauge, and the oxygen concentration monitor, allowing the operator to continuously monitor chamber pressure, airflow, and oxygen levels to ensure safe, accurate, and efficient treatments.
Each component on the Control Panel Console will be explained here.
Air Inlet / Air Outlet Valves
The Air Inlet and Air Outlet Valves give the operator precise control over chamber pressurization and depressurization. The Air Outlet Valve is primarily used to decompress the chamber with a precise rate and allows for more rapid decompression as needed.
Conveniently located on the control panel and inside the chamber as well , the Air Outlet Valve can be operated from both inside and outside the chamber, allowing either the hyperbaric technician or occupant to safely control airflow when needed during treatment or in an emergency.
Oxygen Flow Meter
The Oxygen Flow Meter provides precise control of the medical oxygen delivered to the patient during treatment. Mounted on the exterior control panel, it allows the hyperbaric technician to accurately adjust and monitor oxygen flow without opening the chamber, ensuring safe and effective oxygen administration throughout the treatment.
Its exterior location also provides immediate access to shut off the oxygen supply in the event of an emergency, allowing for a rapid response while maintaining the ability to visualize the patient and ultimatly increased patient safety.
Chamber Door / Door Seal
The chamber door is designed to open inward, meaning it is held securely closed by the pressure inside the chamber rather than by mechanical latches. This simple, pressure-assisted design provides reliable operation while allowing the door to open easily once the chamber has safely returned to atmospheric pressure.
The replaceable door seal creates an airtight barrier between the door and chamber, preventing air leaks during treatment. Because the seal is a serviceable component, it can be inspected, maintained, and replaced as part of routine chamber maintenance to ensure long-term performance..
Chamber Hull Ground Wire
The Chamber Ground Wire is a critical safety feature required by NFPA 99 to help prevent the buildup of static electricity around the hyperbaric chamber. During installation, the chamber is connected to the facility's grounding system to ensure less than one ohm of impedance, providing a safe path for electrical discharge and reducing the risk of ignition in an oxygen-enriched environment.
Patient Grounding Point
The Patient Grounding Point provides a dedicated connection for the patient's grounding wrist strap during treatment. Required by NFPA 99 for all Class B monoplace hyperbaric chambers, this grounding system helps dissipate static electricity from the patient, reducing the risk of static discharge and enhancing safety within the oxygen-enriched treatment environment.
Communication Pass-Through Port
The Communication Pass-Through Port provides a safe connection for approved hyperbaric communication devices during treatment. Designed with a dual USB-C pass-through system, it allows microphones and speakers to operate inside the chamber without introducing batteries or powered electronics, enabling clear communication while maintaining compliance with hyperbaric safety standards.
Antimicrobial Vinyl Mattress
The Antimicrobial Medical-Grade Vinyl Mattress provides a comfortable and supportive treatment surface while meeting the demands of a clinical hyperbaric environment. Constructed from durable, antimicrobial medical-grade vinyl, it complies with NFPA 99 smolder rate requirements and California fire protection standards, while supporting patient comfort, infection control, and long-term durability.
Chamber Skirts
The Chamber Skirts provide a clean, professional appearance by enclosing the area beneath the chamber and concealing wiring and utility connections. The updated skirt design also incorporates an integrated decorative lighting system, enhancing the chamber's overall aesthetic while maintaining easy access for installation and routine maintenance.
Acrylic Windows
The Acrylic Viewports provide excellent visibility into the chamber, allowing operators to continuously observe the patient throughout treatment. The increased number of viewports enhances patient monitoring while allowing more natural light into the chamber, creating a brighter, more open treatment environment that improves both safety and patient comfort.
Hyperbaric
Media Kit
Pictures, videos and literature to aid in the sales process.
Customers have questions, you have the knowlege
Frequently Asked Questions
Chamber Basics
What type of hyperbaric chamber is this?
This is a Class B Monoplace hard-shell hyperbaric chamber. Unlike soft chambers, hard-shell chambers are designed for higher pressure capabilities, greater durability, improved long-term serviceability, and use in more advanced clinical hyperbaric applications.
What pressure does the chamber operate at?
The chamber can operate across a range of treatment pressures depending on the protocol selected by the provider. Pressure is controlled using preset flow-through air valves, allowing the clinic to choose the appropriate ATA setting for the treatment being performed.
What is the maximum ATA capability?
The chamber is designed with a maximum pressure capability of 4.0 ATA. This allows clinics to operate across a wide clinical pressure range, from lower-pressure wellness-style protocols to higher-pressure medical hyperbaric protocols when clinically appropriate. 4.0 ATA would be specifically for diving or research.
Can the patient sit up or only lie down?
Absolutely. The chamber is spacious enough for patients to either lie down comfortably or sit upright during treatment, depending on their preference and clinical needs. Many patients also use bolsters or pillows for additional support, helping them find a comfortable position throughout the treatment session.
Shipping and Delivery
How is the chamber shipped?
Chambers are shipped through Mayflower, a professional freight carrier that has partnered with our manufacturing team for many years and has extensive experience transporting hyperbaric chambers. Their familiarity with the equipment helps ensure each chamber is handled with the care it requires and delivered safely to its destination. Our team coordinates directly with Mayflower throughout the shipping process to provide a smooth delivery experience.
Where does the chamber ship from?
The chamber ships directly from our manufacturing facility in Arizona to your destination. Once manufacturing and final quality inspections are complete, our logistics team coordinates shipment to your clinic or facility and provides tracking and delivery updates throughout the process.
How long does shipping usually take?
Shipping time depends on the customer’s location, freight availability, production timeline, and delivery requirements. Once the chamber is ready to ship, the sales or logistics team will provide the customer with an estimated delivery window and tracking information when available.
Can the patient sit up or only lie down?
The chamber is shipped securely on a pallet and professionally wrapped to protect it during transportation. Each chamber is carefully packaged to help prevent damage in transit while allowing for safe loading, unloading, and delivery to your facility.
Pricing and Purchase Questions
How much does the chamber cost?
The base price of the chamber is $99,000. Final pricing may vary depending on selected accessories, installation requirements, shipping, and any optional upgrades. Sales representatives should always provide customers with the most current approved pricing sheet or formal quotation rather than quoting from memory to ensure accurate pricing.
What is included in the chamber price?
The chamber price typically includes the chamber body, control panel, acrylic viewports, flow-through valve system, vent valve, patient grounding point, chamber grounding connection, medical-grade mattress, and applicable component documentation as well as 1 free training with each chamber purchased. Additional items such as compressor, shipping, installation, training, or accessories may vary by package.
Are there different chamber models or configurations?
Yes. We currently offer both the ATAMOX 40 monoplace chamber and multiplace hyperbaric chambers to accommodate different facility needs. The ATAMOX 40 is an excellent option for facilities treating one patient at a time, while multiplace chambers allow multiple patients to be treated simultaneously and can accommodate a medical attendant when clinically necessary. Our sales team will help determine which chamber best fits your facility, patient volume, treatment goals, and available space.
Are there financing options available?
Yes. We work closely with Brickhouse Capital and Jack Notebart to help customers explore financing options for their hyperbaric chamber purchase. If financing is of interest, our sales team will gladly make the introduction so you can discuss available loan programs, down payment requirements, monthly payment options, and determine the financing solution that best fits your needs.
Installation Questions
What does installation involve?
Installation involves placing the chamber in the approved treatment room, connecting the required air and oxygen systems, verifying grounding, checking the control panel and valve systems, and confirming that the chamber is operating properly. The installer will also review the setup to ensure the chamber is ready for safe use before handoff.
How long does installation take?
Installation is typically completed within one day, depending on the number of chambers being installed and whether the facility is fully prepared before the installation team arrives.
Who installs the chamber?
The chamber should be installed by a trained installer or qualified technician familiar with hyperbaric chamber setup, pressure systems, oxygen systems, grounding requirements, and manufacturer specifications as well as insured. Installation should not be handled by general maintenance staff unless they have been specifically trained and approved for this type of equipment.
Does the chamber require special electrical work?
The chamber itself does not require complex electrical work, but the supporting equipment does require adequate power. Each compressor operates from a standard 20-amp electrical outlet. Facilities installing multiple chambers with several compressors should evaluate their available electrical capacity, as additional circuits or electrical service may be needed. The facility should also ensure proper grounding in accordance with NFPA 99 and the manufacturer's installation requirements.