Carefusion 209, Inc.

Carefusion 209, Inc. — FDA 510(k) Submissions

Carefusion 209, Inc. has submitted 5 FDA 510(k) premarket notifications since 2011, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode, Needle, Diagnostic Electromyograph, Stimulator, Electrical, Evoked Response, Amplifier, Physiological Signal . Use the specialty filter in the sidebar to narrow results.