FDA 510(k) Applications Submitted by C. R. Bard, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K181323 |
05/18/2018 |
Atlas Gold PTA Dilatation Catheter |
C. R. Bard, Inc. |
| K152613 |
09/14/2015 |
True Flow Valvuloplasty Perfusion Catheter |
C. R. BARD, INC. |
| K172932 |
09/26/2017 |
True Flow Valvuloplasty Perfusion Catheter |
C. R. Bard, Inc. |
| K103459 |
11/24/2010 |
VASCUTRAK PTA DILATATION CATHETER |
C. R. BARD, INC. |
| K170158 |
01/18/2017 |
PowerGlide ST Midline Catheter |
C. R. Bard, Inc. |
| K163437 |
12/07/2016 |
hypodermic PinpointÖ GT Needle |
C. R. Bard, Inc. |
| K213203 |
09/29/2021 |
Provena(TM) Midline Catheter |
C. R. Bard, Inc. |
| K182796 |
10/01/2018 |
WavelinQ 4F EndoAVF System |
C. R. Bard, Inc. |
| K191532 |
06/10/2019 |
The Caterpillar and Caterpillar Micro Arterial Embolization Devices |
C. R. Bard, Inc. |
| K180781 |
03/26/2018 |
Bard Vertus Foley Catheter |
C. R. Bard, Inc. |
|
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