Travenol Laboratories, S.A.

Travenol Laboratories, S.A. — FDA 510(k) Submissions

Travenol Laboratories, S.A. has submitted 206 FDA 510(k) premarket notifications since 1976, of which 206 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Infusion, Set, Administration, Intravascular, Set, Administration, For Peritoneal Dialysis, Disposable, Humidifier, Respiratory Gas, (direct Patient Interface), Nebulizer (direct Patient Interface) . Use the specialty filter in the sidebar to narrow results.