Medical Device Manufacturer · US , Mt. Laurel , NJ

Sopro - Acteon Group - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

Sopro - Acteon Group has 4 FDA 510(k) cleared medical devices. Based in Mt. Laurel, US.

Historical record: 4 cleared submissions from 2014 to 2016. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Sopro - Acteon Group

4 devices

1-4 of 4