Pneu-Mobility, Inc.
Country not established
- Devices
- 1
What Pneu-Mobility, Inc. makes
Pneu-Mobility, Inc. manufactures the PNEU-WAVE, a medical device designed for respiratory support or mobility assistance in clinical settings.
The PNEU-WAVE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Pneu-Wave Ref K911574
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pneu-Mobility, Inc. have in the registry?
The registry currently lists 1 device for Pneu-Mobility, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneu-Mobility, Inc.'s devices?
Among its 1 most recently registered device, Pneu-Mobility, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pneu-Mobility, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pneu-Mobility, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneu-Mobility, Inc. in the registry?
The most recently registered devices listed for Pneu-Mobility, Inc. include PNEU-WAVE.