Vitrolife GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vitrolife GmbH has 1 FDA 510(k) cleared medical devices. Based in Bruckberg, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Vitrolife GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Vitrolife GmbH
1 devices