Vitrolife AB is one of 17876 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vitrolife AB - FDA 510(k) Cleared Devices
Recent clearances: G-FREEZEKIT BLAST, G-THAWKIT BLAST, PERFADEX SOLUTION FOR LUNG PRESERVATION
3
Total
3
Cleared
0
Denied
Vitrolife AB has 3 FDA 510(k) cleared medical devices. Based in Ringoes, US.
Historical record: 3 cleared submissions from 2003 to 2004. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Vitrolife AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vitrolife AB
3 devices