Medical Device Manufacturer · US , San Diego , CA

Braemar Manufacturing, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2013

Total

Cleared

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

1-3 of 3