Vygon

Vygon — FDA 510(k) Submissions

Vygon has submitted 2 FDA 510(k) premarket notifications since 2014, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Enteral Specific Transition Connectors . Use the specialty filter in the sidebar to narrow results.