Belimed Sauter AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Belimed Sauter AG - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Belimed Sauter AG has 3 FDA 510(k) cleared medical devices. Based in Sulgen (Tg), CH.
Historical record: 3 cleared submissions from 2007 to 2010. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Belimed Sauter AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Belimed Sauter AG
3 devices