Arrow International, LLC Subsidiary of Teleflex Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, LLC Subsidiary of Teleflex Incorporated - FDA 51...
Recent clearances: Arrow Pressure Injectable Midline Catheter
1
Total
1
Cleared
0
Denied
Arrow International, LLC Subsidiary of Teleflex Incorporated has 1 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arrow International, LLC Subsidiary of Teleflex Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrow International, LLC Subsidiary of Teleflex Incorporated
1 devices