Medical Device Manufacturer · US , New Brighton , MN

Rehabilicare, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1997

Total

Cleared

Denied

Rehabilicare, Inc. has 4 FDA 510(k) cleared medical devices. Based in New Brighton, US.

Historical record: 4 cleared submissions from 1997 to 2002. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Rehabilicare, Inc. Filter by specialty or product code using the sidebar.

Rehabilicare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Rehabilicare, Inc.

4 devices

1-4 of 4