Medical Device Manufacturer · DE , Bruckberg

Vitrolife GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2020

Recent clearances: LaserShot M, NaviLase

1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Vitrolife GmbH Obstetrics & Gynecology

1 devices
1-1 of 1
Filters