Medical Device Manufacturer · US , Reading , PA

Arrow International, Inc. (Subsidiary of Teleflex, Inc.) - FDA 510(k)...

8 submissions · 7 cleared · Since 2015

Recent clearances: EZ-IO Intraosseous Vascular Access System, Arrow Endurance Extended Dwell Peripheral Catheter System, ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and Antithrombogenic Technology

Total

Cleared

Denied

Arrow International, Inc. (Subsidiary of Teleflex, Inc.) has 7 FDA 510(k) cleared medical devices. Based in Reading, US.

Historical record: 7 cleared submissions from 2015 to 2018. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Arrow International, Inc. (Subsidiary of Teleflex, Inc.) Filter by specialty or product code using the sidebar.

1 device has linked clinical trial registered on ClinicalTrials.gov.

Arrow International, Inc. (Subsidiary of Teleflex, Inc.) is one of 15106 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.