Micromed S.P.A.

Micromed S.P.A. — FDA 510(k) Submissions

Micromed S.P.A. has submitted 4 FDA 510(k) premarket notifications since 2008, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Full-montage Standard Electroencephalograph, Electrode, Cortical, Stimulator, Photic, Evoked Response, Standard Polysomnograph With Electroencephalograph . Use the specialty filter in the sidebar to narrow results.