Servox Medizintechnik GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Servox Medizintechnik GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Servox Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Koln, DE.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Servox Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Servox Medizintechnik GmbH
1 devices