Arrow International, Inc. (Subsidiary of Teleflex, Inc.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, Inc. (Subsidiary of Teleflex, Inc.) - FDA 510(k)...
Recent clearances: EZ-IO Intraosseous Vascular Access System
8
Total
7
Cleared
0
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.
FDA 510(k) Regulatory Record - Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
8 devices
Cleared
CT
Nov 09, 2018
EZ-IO Intraosseous Vascular Access System
General Hospital
269d
Cleared
Feb 24, 2017
Arrow Endurance Extended Dwell Peripheral Catheter System
General Hospital
71d
Cleared
Aug 24, 2016
ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and...
General Hospital
106d
Cleared
Jun 13, 2016
Arrow Quickflash Arterial Catheterization Device
Cardiovascular
160d
Cleared
Feb 04, 2016
CG+ Arrow PICC powered by Arrow VPS Stylet PLUS and Arrow VPS Stylet PLUS
General Hospital
62d
Cleared
Jan 28, 2016
CG+ Arrow JACC powered by Arrow VPS Stylet, CG+ Arrow JACC
General Hospital
64d
Cleared
Nov 23, 2015
Arrow Endurance Extended Dwell Peripheral Catheter System
General Hospital
103d
Cleared
Jul 24, 2015
Multi-Lumen Acute Hemodialysis Catheter for High Volume Infusions
Gastroenterology & Urology
268d