Medical Device Manufacturer · SE , Sweden

Abigo Medical AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

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

Historical record: 5 cleared submissions from 1992 to 2017. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Abigo Medical AB

5 devices

1-5 of 5