Vitasystems GmbH is one of 490 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vitasystems GmbH - FDA 510(k) Cleared Devices
Recent clearances: EMMa Electronic Monitoring Management, Vitaphone Tele ECG Loop Recorder, VITAPHONE. MODEL 100 BT
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vitasystems GmbH
3 devices