Gulf Coast Hyperbarics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Gulf Coast Hyperbarics, Inc. makes
Gulf Coast Hyperbarics, Inc. makes hyperbaric treatment systems, including multiplace hyperbaric treatment chamber systems and rectangular multiplace hyperbaric chambers, as well as infant oxygen treatment hoods. These products are medical devices used for hyperbaric oxygen therapy.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Multiplace Hyperbaric Treatment Chamber System Ref K950957
Regimes: 510(k) Registry: 510(k)Infant Oxygen Treatment Hood Ref K011565
Regimes: 510(k) Registry: 510(k)Rectangular Multiplace Hyperbaric Chamber Ref K082455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gulf Coast Hyperbarics, Inc. have in the registry?
The registry currently lists 3 devices for Gulf Coast Hyperbarics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gulf Coast Hyperbarics, Inc.'s devices?
Among its 3 most recently registered devices, Gulf Coast Hyperbarics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Gulf Coast Hyperbarics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Gulf Coast Hyperbarics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gulf Coast Hyperbarics, Inc. in the registry?
The most recently registered devices listed for Gulf Coast Hyperbarics, Inc. include MULTIPLACE HYPERBARIC TREATMENT CHAMBER SYSTEM, INFANT OXYGEN TREATMENT HOOD and RECTANGULAR MULTIPLACE HYPERBARIC CHAMBER.