Sapimed S.P.A.

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

Sapimed S.P.A. 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 Ligator, Hemorrhoidal, Anoscope And Accessories, Sigmoidoscope, Rigid, Non-electrical . Use the specialty filter in the sidebar to narrow results.