Cordis Corp.

Cordis Corp. — FDA 510(k) Submissions

Cordis Corp. has submitted 315 FDA 510(k) premarket notifications since 1976, of which 281 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stents, Drains And Dilators For The Biliary Ducts, Catheter, Intravascular, Diagnostic, Catheter, Angioplasty, Peripheral, Transluminal, Wire, Guide, Catheter, Catheter, Percutaneous . Use the specialty filter in the sidebar to narrow results.