Med Air Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Adjustable Peep Valve Ref K872202
Regimes: 510(k) Registry: 510(k)Hy-Flow Non-Rebreathing Valve Assembly Ref K871367
Regimes: 510(k) Registry: 510(k)Variable High Flow Downs Cpap Generator Ref K861104
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med Air Technology, Inc. have in the registry?
The registry currently lists 3 devices for Med Air Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med Air Technology, Inc.'s devices?
Among its 3 most recently registered devices, Med Air Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Med Air Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Med Air Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med Air Technology, Inc. in the registry?
The most recently registered devices listed for Med Air Technology, Inc. include ADJUSTABLE PEEP VALVE, HY-FLOW NON-REBREATHING VALVE ASSEMBLY and VARIABLE HIGH FLOW DOWNS CPAP GENERATOR.