Vitasystems GmbH is one of 199 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vitasystems GmbH - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Vitasystems GmbH has 3 FDA 510(k) cleared medical devices. Based in Chemnitz, DE.
Historical record: 3 cleared submissions from 2010 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vitasystems GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vitasystems GmbH
3 devices