Cordis US Corp

Cordis US Corp — FDA 510(k) Submissions

Cordis US Corp has submitted 4 FDA 510(k) premarket notifications since 2022, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Angioplasty, Peripheral, Transluminal, Introducer, Catheter, Catheter, Intravascular, Diagnostic, Catheter, Percutaneous . Use the specialty filter in the sidebar to narrow results.