Medical Device Manufacturer · FR , Valbonne

Median Technologies

3 submissions · 3 cleared · Since 2007
3
Total
3
Cleared
0
Denied

Median Technologies — FDA 510(k) Submissions

Median Technologies has submitted 3 FDA 510(k) premarket notifications since 2007, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Image Processing, Radiological, Radiological Computer Assisted Detection/diagnosis Software For Lesions Suspicious For Cancer . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
All3 Radiology 3