Lung Assist, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Lung Assist, Inc. makes
Lung Assist, Inc. makes the Vital Cough device, which is a respiratory support product designed to assist with airway clearance.
The Vital Cough device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Vital Cough Ref K120277
Regimes: 510(k) Registry: 510(k)Vital Cough Ref K132988
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lung Assist, Inc. have in the registry?
The registry currently lists 2 devices for Lung Assist, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lung Assist, Inc.'s devices?
Among its 2 most recently registered devices, Lung Assist, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lung Assist, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lung Assist, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lung Assist, Inc. in the registry?
The most recently registered devices listed for Lung Assist, Inc. include VITAL COUGH.