Medical Device Manufacturer · FR , La Tronche

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

2 submissions · 2 cleared · Since 2007
2
Total
2
Cleared
0
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.

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