Teleflex, Inc.

Teleflex, Inc. — FDA 510(k) Submissions

Teleflex, Inc. has submitted 10 FDA 510(k) premarket notifications since 1986, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Anesthesia Conduction Kit, Introducer, Catheter, Humidifier, Respiratory Gas, (direct Patient Interface), Catheter, Conduction, Anesthetic . Use the specialty filter in the sidebar to narrow results.