Biowatch Medical, Inc.
Country not established
- Devices
- 1
What Biowatch Medical, Inc. makes
Biowatch Medical, Inc. manufactures the VST3, a medical device designed for vascular surgery applications, including the creation and management of vascular access sites.
The VST3 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
VST3 Ref K040942
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biowatch Medical, Inc. have in the registry?
The registry currently lists 1 device for Biowatch Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biowatch Medical, Inc.'s devices?
Among its 1 most recently registered device, Biowatch Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biowatch Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biowatch Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biowatch Medical, Inc. in the registry?
The most recently registered devices listed for Biowatch Medical, Inc. include VST3.