Medical Device Manufacturer · US , Allentown , PA

B.Braun Melsungen AG - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2011

Total

Cleared

Denied

B.Braun Melsungen AG has 5 FDA 510(k) cleared medical devices. Based in Allentown, US.

Historical record: 5 cleared submissions from 2011 to 2017. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by B.Braun Melsungen AG Filter by specialty or product code using the sidebar.

B.Braun Melsungen AG is one of 4723 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - B.Braun Melsungen AG

5 devices

1-5 of 5