Medical Device Manufacturer · US , Burnsville , MN

Braemar Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Braemar Corp. has 5 FDA 510(k) cleared medical devices. Based in Burnsville, US.

Historical record: 5 cleared submissions from 1995 to 2003. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Braemar Corp. Filter by specialty or product code using the sidebar.

Braemar Corp. 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 - Braemar Corp.

5 devices

1-5 of 5