Myomed, Inc.
Country not established
- Devices
- 1
What Myomed, Inc. makes
Myomed, Inc. manufactures the ACCU-O-MATIC, a device designed for monitoring and managing muscle stimulation therapy, likely used in physical rehabilitation or neuromuscular applications.
The ACCU-O-MATIC is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Accu-O-Matic Ref K841427
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Myomed, Inc. have in the registry?
The registry currently lists 1 device for Myomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Myomed, Inc.'s devices?
Among its 1 most recently registered device, Myomed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Myomed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Myomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Myomed, Inc. in the registry?
The most recently registered devices listed for Myomed, Inc. include ACCU-O-MATIC.