Spes Medica Srl

Spes Medica Srl — FDA 510(k) Submissions

Spes Medica Srl has submitted 9 FDA 510(k) premarket notifications since 2009, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Electroconductive, Stimulator, Nerve, Electrode, Needle, Diagnostic Electromyograph, Electrode, Cutaneous, Electrode, Needle . Use the specialty filter in the sidebar to narrow results.