Nunc A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Nunc A/S - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Nunc A/S has 2 FDA 510(k) cleared medical devices. Based in Roskilde, DK.
Historical record: 2 cleared submissions from 2004 to 2007. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Nunc A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nunc A/S
2 devices