Carefusion 303, Inc.

Carefusion 303, Inc. — FDA 510(k) Submissions

Carefusion 303, Inc. has submitted 7 FDA 510(k) premarket notifications since 2011, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pump, Infusion, Transmitters And Receivers, Physiological Signal, Radiofrequency, Cable, Transducer And Electrode, Patient, (including Connector), Set, Administration, Intravascular . Use the specialty filter in the sidebar to narrow results.