Air Plus, Inc.
Country not established
- Devices
- 1
What Air Plus, Inc. makes
Air Plus, Inc. makes air fluidized therapy systems.
These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Air Plus Air Fluidized Therapy Systems Ref K852036
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Air Plus, Inc. have in the registry?
The registry currently lists 1 device for Air Plus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Air Plus, Inc.'s devices?
Among its 1 most recently registered device, Air Plus, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Air Plus, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Air Plus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Air Plus, Inc. in the registry?
The most recently registered devices listed for Air Plus, Inc. include AIR PLUS AIR FLUIDIZED THERAPY SYSTEMS.