Scandimed International is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Scandimed International - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Scandimed International has 2 FDA 510(k) cleared medical devices. Based in Glostrop, DK.
Historical record: 2 cleared submissions from 2008 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Scandimed International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scandimed International
2 devices