Medical Device Manufacturer · FR , La Tronche

Praxim Medivision, SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Praxim Medivision, SA has 2 FDA 510(k) cleared medical devices. Based in La Tronche, FR.

Historical record: 2 cleared submissions from 2007 to 2010. Primary specialty: Neurology.

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

Praxim Medivision, SA is one of 255 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Praxim Medivision, SA

2 devices

1-2 of 2