Arrow International, Inc. - FDA 510(k) Cleared Devices
19
Total
17
Cleared
0
Denied
Arrow International, Inc. has 17 FDA 510(k) cleared medical devices. Based in Reading, US.
Historical record: 17 cleared submissions from 2003 to 2020.
Browse the FDA 510(k) cleared devices submitted by Arrow International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Arrow International, Inc.
19 devices
Cleared
May 27, 2020
AC3 IABP, AC3 Optimus IABP, AutoCAT2 Wave IABP, AutoCAT2 IABP
Cardiovascular
30d
Cleared
Apr 09, 2020
Arrow FiberOptix Intra-Aortic Balloon Catheter Kit
Cardiovascular
30d
Cleared
Jun 28, 2019
UltraFlex IAB
Cardiovascular
157d
Cleared
Jun 13, 2019
Fiberoptix IAB
Cardiovascular
140d
Cleared
Mar 31, 2017
AC3 Series IABP System
Cardiovascular
175d
Cleared
Jul 07, 2014
VECTORFLOW
Gastroenterology & Urology
74d
Cleared
May 10, 2013
NEXTSTEP RETROGRADE
Gastroenterology & Urology
105d
Cleared
Apr 26, 2013
CG+ ARROW PICC POWERED BY ARROW VPS STYLET
General Hospital
28d
Cleared
Dec 21, 2012
ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE
Anesthesiology
108d
Cleared
Aug 28, 2012
ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER
Anesthesiology
48d
Cleared
Jun 21, 2012
ARROWADVANTAGES PRESSURE INJECTABLE PERIPHERALLY INSCRTED CENTRAL CATHETER KITS
General Hospital
227d
Cleared
Jun 27, 2008
PRESSURE INJFECTABLE PICC
General Hospital
115d
Cleared
Jan 15, 2008
PRESSURE INJECTABLE PICC
General Hospital
36d
Cleared
Aug 30, 2007
ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS...
General Hospital
86d
Cleared
Aug 24, 2006
ARROW PRESSURE INJECTABLE PICC
General Hospital
107d
Cleared
Oct 15, 2004
SILICONE COATED GUIDEWIRE
Cardiovascular
109d
Cleared
May 14, 2004
STEP-TIP CHRONIC HEMODIALYSIS CATHETER
Gastroenterology & Urology
60d
Cleared
Feb 13, 2004
CANNON II PLUS
Gastroenterology & Urology
30d
Cleared
Apr 23, 2003
STIMUCATH CONTINUOUS NERVE BLOCK SET, MODELS AB-02030, AB-02060, AB-02090,...
Anesthesiology
29d