Medical Device Manufacturer · FR , Paris

Visiomed Group SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Visiomed Group SA has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.

Historical record: 2 cleared submissions from 2011 to 2018. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Visiomed Group SA Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Visiomed Group SA

2 devices

1-2 of 2