B. Braun Melsugen AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
B. Braun Melsugen AG - FDA 510(k) Cleared Devices
Recent clearances: SpaceStation MRI
1
Total
1
Cleared
0
Denied
B. Braun Melsugen AG has 1 FDA 510(k) cleared medical devices. Based in Melsungen, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by B. Braun Melsugen AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - B. Braun Melsugen AG
1 devices