O-Matic, Inc.
Country not established
- Devices
- 1
What O-Matic, Inc. makes
O-Matic, Inc. manufactures the TENS-O-MATIC, which is a transcutaneous electrical nerve stimulation device.
This device is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Tens-O-Matic Ref K811012
510(k) 510(k)
Frequently asked questions
How many devices does O-Matic, Inc. have in the registry?
The registry currently lists 1 device for O-Matic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list O-Matic, Inc.'s devices?
Among its 1 most recently registered device, O-Matic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do O-Matic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for O-Matic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from O-Matic, Inc. in the registry?
The most recently registered devices listed for O-Matic, Inc. include TENS-O-MATIC.