Medical Device Manufacturer · CH , Port

Sis Ag, Surgical Instrument Systems - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2019

Total

Cleared

Denied

Sis Ag, Surgical Instrument Systems has 1 FDA 510(k) cleared medical devices. Based in Port, CH.

Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Sis Ag, Surgical Instrument Systems Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Sis Ag, Surgical Instrument Systems

1 devices

1-1 of 1