Medical Device Manufacturer · SE , Sweden

Artema Medical AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1991

Total

Cleared

Denied

Artema Medical AB has 5 FDA 510(k) cleared medical devices. Based in Sweden, SE.

Historical record: 5 cleared submissions from 1991 to 1995. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Artema Medical AB Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Artema Medical AB

5 devices

1-5 of 5