Sis Medical AG - FDA 510(k) Cleared Devices

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.