Watlow/Winona, Inc.
Country not established
- Devices
- 1
What Watlow/Winona, Inc. makes
Watlow/Winona, Inc. manufactures the MEDA 2500 T.E.N.S. device, a transcutaneous electrical nerve stimulation (TENS) unit designed for pain management applications.
The MEDA 2500 T.E.N.S. is classified as a Class II medical device and is listed under FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Meda 2500 T.E.N.S. Ref K862450
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Watlow/Winona, Inc. have in the registry?
The registry currently lists 1 device for Watlow/Winona, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Watlow/Winona, Inc.'s devices?
Among its 1 most recently registered device, Watlow/Winona, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Watlow/Winona, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Watlow/Winona, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Watlow/Winona, Inc. in the registry?
The most recently registered devices listed for Watlow/Winona, Inc. include MEDA 2500 T.E.N.S..