American Biosystems, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Abi Vest Airway Clearance System Ref K993629
Regimes: 510(k) Registry: 510(k)Thairapy Vest System Ref K965192
Regimes: 510(k) Registry: 510(k)Thairapy System Ref K936121
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Biosystems, Inc. have in the registry?
The registry currently lists 4 devices for American Biosystems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Biosystems, Inc.'s devices?
Among its 4 most recently registered devices, American Biosystems, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do American Biosystems, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for American Biosystems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Biosystems, Inc. in the registry?
The most recently registered devices listed for American Biosystems, Inc. include ABI VEST AIRWAY CLEARANCE SYSTEM, THAIRAPY VEST SYSTEM, THAIRAPY SYSTEM and THAIRAPY(TM) BRONCHIAL DRAINAGE SYSTEM, MODEL 101.