Dept. of the Navy
Country not established
- Devices
- 1
What Dept. of the Navy makes
The manufacturer produces portable, volume-controlled respirators designed for medical use, intended to assist patients with breathing support in clinical settings.
These devices are classified as Class II under US regulations and are listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Respirator, Protable, Volume Controlled Ref K771039
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dept. of the Navy have in the registry?
The registry currently lists 1 device for Dept. of the Navy. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dept. of the Navy's devices?
Among its 1 most recently registered device, Dept. of the Navy has devices listed in FDA 510(k) (1 device).
What risk classes do Dept. of the Navy's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dept. of the Navy's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dept. of the Navy in the registry?
The most recently registered devices listed for Dept. of the Navy include RESPIRATOR, PROTABLE, VOLUME CONTROLLED.