Tampa Hyperbaric Ent.
Country not established
- Devices
- 2
What Tampa Hyperbaric Ent. makes
Tampa Hyperbaric Ent. manufactures hyperbaric chambers, including a standard hyperbaric chamber and the Tampa Hyperbaric Monoplace Chamber, which are single‑patient, pressurized treatment units used for therapeutic oxygen therapy.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Hyperbaric Chamber Ref K960389
Regimes: 510(k) Registry: 510(k)Tampa Hyperbaric Monoplace Chamber Ref K981938
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tampa Hyperbaric Ent. have in the registry?
The registry currently lists 2 devices for Tampa Hyperbaric Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tampa Hyperbaric Ent.'s devices?
Among its 2 most recently registered devices, Tampa Hyperbaric Ent. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tampa Hyperbaric Ent.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tampa Hyperbaric Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tampa Hyperbaric Ent. in the registry?
The most recently registered devices listed for Tampa Hyperbaric Ent. include HYPERBARIC CHAMBER and TAMPA HYPERBARIC MONOPLACE CHAMBER.