Arrow International, LLC (A subsidiary of Teleflex, Inc.)

Arrow International, LLC (A subsidiary of Teleflex, Inc.) — FDA 510(k) Submissions

Arrow International, LLC (A subsidiary of Teleflex, Inc.) has submitted 4 FDA 510(k) premarket notifications since 2022, of which 4 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, Stylet, Catheter, Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days . Use the specialty filter in the sidebar to narrow results.