Median Technologies

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.