Braemar Manufacturing, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Braemar Manufacturing, LLC - FDA 510(k) Cleared Devices
Recent clearances: ePatch
3
Total
3
Cleared
0
Denied
Braemar Manufacturing, LLC has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 3 cleared submissions from 2013 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Braemar Manufacturing, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Braemar Manufacturing, LLC
3 devices