Arrow Pressure Injectable Midline Catheter
Sep 2022
266d
Arrow International, LLC Subsidiary of Teleflex Incorporated
1
Total
1
Cleared
0
Denied
Arrow International, LLC Subsidiary of Teleflex Incorporated — FDA 510(k) Submissions
Arrow International, LLC Subsidiary of Teleflex Incorporated has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Midline Catheter . Use the specialty filter in the sidebar to narrow results.
1 devices