Promepla Sam

Promepla Sam — FDA 510(k) Submissions

Promepla Sam has submitted 5 FDA 510(k) premarket notifications since 2012, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accessories, Catheter, G-u, Endoscopic Irrigation/suction System, Stent, Ureteral . Use the specialty filter in the sidebar to narrow results.