Versatec, Inc.
Country not established
- Devices
- 1
What Versatec, Inc. makes
Versatec, Inc. manufactures the Versatec 310 Electrode, a reusable electrode designed for use in electrotherapy applications, including transcutaneous electrical nerve stimulation (TENS) and muscle stimulation therapies.
The Versatec 310 Electrode is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Versatec 310 Electrode Ref K963975
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Versatec, Inc. have in the registry?
The registry currently lists 1 device for Versatec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Versatec, Inc.'s devices?
Among its 1 most recently registered device, Versatec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Versatec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Versatec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Versatec, Inc. in the registry?
The most recently registered devices listed for Versatec, Inc. include VERSATEC 310 ELECTRODE.