Scandimed. A.S. is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Scandimed. A.S. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Scandimed. A.S. has 2 FDA 510(k) cleared medical devices. Based in Glostrop, DK.
Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Scandimed. A.S. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scandimed. A.S.
2 devices