Arrow Internation, Inc. (Subsidiary of Teleflex Inc.) is one of 18988 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow Internation, Inc. (Subsidiary of Teleflex Inc.) - FDA 510(k) Cl...
Recent clearances: Arrow Endurance Extended Dwell Peripheral Catheter System
1
Total
1
Cleared
0
Denied
Arrow Internation, Inc. (Subsidiary of Teleflex Inc.) has 1 FDA 510(k) cleared medical devices. Based in Reading, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arrow Internation, Inc. (Subsidiary of Teleflex Inc.) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Arrow Internation, Inc. (Subsidiary of Teleflex Inc.)
1 devices