Meadox Medicals, Div. Boston Scientific Corp.

Meadox Medicals, Div. Boston Scientific Corp. — FDA 510(k) Submissions

Meadox Medicals, Div. Boston Scientific Corp. has submitted 53 FDA 510(k) premarket notifications since 1976, of which 47 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Vascular Graft, Of 6mm And Greater Diameter, Catheter, Angioplasty, Peripheral, Transluminal, Wire, Guide, Catheter, Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene, Dilator, Catheter, Ureteral . Use the specialty filter in the sidebar to narrow results.