Wisap/U.S.A.
Country not established
- Devices
- 1
What Wisap/U.S.A. makes
Wisap/U.S.A. makes the OP-PNEU ELECTRONIC CO2 device.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Op-Pneu Electronic CO2 Ref K941438
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wisap/U.S.A. have in the registry?
The registry currently lists 1 device for Wisap/U.S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wisap/U.S.A.'s devices?
Among its 1 most recently registered device, Wisap/U.S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Wisap/U.S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wisap/U.S.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wisap/U.S.A. in the registry?
The most recently registered devices listed for Wisap/U.S.A. include OP-PNEU ELECTRONIC CO2.