FDA 510(k) Applications Submitted by ARROW INTERNATIONAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K162820 |
10/07/2016 |
AC3 Series IABP System |
ARROW INTERNATIONAL, INC. |
| K040078 |
01/14/2004 |
CANNON II PLUS |
ARROW INTERNATIONAL, INC. |
| K040666 |
03/15/2004 |
STEP-TIP CHRONIC HEMODIALYSIS CATHETER |
ARROW INTERNATIONAL, INC. |
| K030937 |
03/25/2003 |
STIMUCATH CONTINUOUS NERVE BLOCK SET, MODELS AB-02030, AB-02060, AB-02090, AB-02030-PK, AB-02060-PK, AB-02090-PK |
ARROW INTERNATIONAL, INC. |
| K130876 |
03/29/2013 |
CG+ ARROW PICC POWERED BY ARROW VPS STYLET |
ARROW INTERNATIONAL, INC. |
| K061289 |
05/09/2006 |
ARROW PRESSURE INJECTABLE PICC |
ARROW INTERNATIONAL, INC. |
| K141051 |
04/24/2014 |
VECTORFLOW; ANTEGRADE CHRONIC HEMODIALYSIS CATHETER, RETROGRADE CHRONIC HEMODIALYSIS CATHETER, RETROGRADE REPLACEMENT HU |
ARROW INTERNATIONAL, INC. |
| K130192 |
01/25/2013 |
NEXTSTEP RETROGRADE |
ARROW INTERNATIONAL, INC. |
| K080604 |
03/04/2008 |
PRESSURE INJFECTABLE PICC |
ARROW INTERNATIONAL, INC. |
| K073451 |
12/10/2007 |
PRESSURE INJECTABLE PICC |
ARROW INTERNATIONAL, INC. |
| K071538 |
06/05/2007 |
ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER |
ARROW INTERNATIONAL, INC. |
| K190101 |
01/22/2019 |
UltraFlex IAB |
Arrow International, Inc. |
| K190117 |
01/24/2019 |
Fiberoptix IAB |
Arrow International, Inc. |
| K122027 |
07/11/2012 |
ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER |
ARROW INTERNATIONAL, INC. |
| K122690 |
09/04/2012 |
ULTRAQUIK PERIPHERAL NERVE BLOCK NEEDLE |
ARROW INTERNATIONAL, INC. |
| K041740 |
06/28/2004 |
SILICONE COATED GUIDEWIRE |
ARROW INTERNATIONAL, INC. |
| K113277 |
11/07/2011 |
ARROWADVANTAGES PRESSURE INJECTABLE PERIPHERALLY INSCRTED CENTRAL CATHETER KITS |
ARROW INTERNATIONAL, INC. |
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