Becton Dickinson Vascular Access, Inc.

Becton Dickinson Vascular Access, Inc. — FDA 510(k) Submissions

Becton Dickinson Vascular Access, Inc. has submitted 25 FDA 510(k) premarket notifications since 1992, of which 22 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, Set, Administration, Intravascular, Transducer, Pressure, Catheter Tip, Catheter, Irrigation, Introducer, Catheter . Use the specialty filter in the sidebar to narrow results.