Weston, Copco, Inc.
Country not established
- Devices
- 1
What Weston, Copco, Inc. makes
Weston, Copco, Inc. manufactures the VAKUTAGE, a medical device designed for vacuum-assisted wound closure and drainage.
The VAKUTAGE is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Vakutage Ref K823080
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Weston, Copco, Inc. have in the registry?
The registry currently lists 1 device for Weston, Copco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Weston, Copco, Inc.'s devices?
Among its 1 most recently registered device, Weston, Copco, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Weston, Copco, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Weston, Copco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Weston, Copco, Inc. in the registry?
The most recently registered devices listed for Weston, Copco, Inc. include VAKUTAGE.