Sis Medical AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Sis Medical AG - FDA 510(k) Cleared Devices
Recent clearances: OPN NC PTCA Dilatation Catheter
1
Total
1
Cleared
0
Denied
Sis Medical AG has 1 FDA 510(k) cleared medical devices. Based in Frauenfeld, CH.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sis Medical AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cardiomed Device Consultants as regulatory consultant.
FDA 510(k) Regulatory Record - Sis Medical AG
1 devices