Medical Device Manufacturer · US , Rochester , NY

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

3 submissions · 3 cleared · Since 1982

Total

Cleared

Denied

Rabar, Inc. has 3 FDA 510(k) cleared medical devices. Based in Rochester, US.

Historical record: 3 cleared submissions from 1982 to 1984. Primary specialty: Neurology.

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

Rabar, 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 - Rabar, Inc.

3 devices

1-3 of 3