Vitalitec Medizintechnik GmbH is one of 490 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vitalitec Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: Kerrison Rongeurs
1
Total
1
Cleared
0
Denied
Vitalitec Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Balgheim (Baden-Wurttem Berg), DE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Vitalitec Medizintechnik GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lyle Howard Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Vitalitec Medizintechnik GmbH
1 devices