Medical Device Manufacturer · US , Washington , DC

Vitrolife AB/Scandinavian Ivf Sciences AB - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000

Total

Cleared

Denied

Vitrolife AB/Scandinavian Ivf Sciences AB has 7 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 7 cleared submissions from 2000 to 2000. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Vitrolife AB/Scandinavian Ivf Sciences AB Filter by specialty or product code using the sidebar.

Vitrolife AB/Scandinavian Ivf Sciences AB is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Vitrolife AB/Scandinavian Ivf Sciences AB

7 devices

1-7 of 7