Urotech U.S.A., Inc.
Country not established
- Devices
- 1
What Urotech U.S.A., Inc. makes
Urotech U.S.A., Inc. manufactures the Urotech Catheter, a medical device designed for urinary drainage and catheterization purposes.
The device falls under FDA Class II regulation and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Urotech Catheter Ref K911617
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Urotech U.S.A., Inc. have in the registry?
The registry currently lists 1 device for Urotech U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Urotech U.S.A., Inc.'s devices?
Among its 1 most recently registered device, Urotech U.S.A., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Urotech U.S.A., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Urotech U.S.A., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Urotech U.S.A., Inc. in the registry?
The most recently registered devices listed for Urotech U.S.A., Inc. include UROTECH CATHETER.