Gebr. Brasseler GmbH & Co. KG - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Gebr. Brasseler GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Lemgo, DE.
Historical record: 2 cleared submissions from 2007 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Gebr. Brasseler GmbH & Co. KG Filter by specialty or product code using the sidebar.
2 devices