Bimed, Inc.
Country not established
- Devices
- 1
What Bimed, Inc. makes
Bimed, Inc. manufactures the BIOFEEDBACK BIO 80, a device designed for biofeedback therapy to assist in physiological monitoring and patient training.
The BIOFEEDBACK BIO 80 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Biofeedback Bio 80 Ref K803099
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bimed, Inc. have in the registry?
The registry currently lists 1 device for Bimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bimed, Inc.'s devices?
Among its 1 most recently registered device, Bimed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bimed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bimed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bimed, Inc. in the registry?
The most recently registered devices listed for Bimed, Inc. include BIOFEEDBACK BIO 80.