Rehab Medical Specialties, Inc. is one of 25989 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rehab Medical Specialties, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SOKEN PLUS(TM) ELECTRONIC MUSCLE STIMULATOR, SOKEN(TM) ELECTRONIC MUSCLE STIMULATOR, MULTIPLE SOKEN 3 ELECTRON-MUSCLE STIM
3
Total
3
Cleared
0
Denied
Rehab Medical Specialties, Inc. has 3 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 3 cleared submissions from 1983 to 1989. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Rehab Medical Specialties, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rehab Medical Specialties, Inc.
3 devices