FDA 510(k) Applications Submitted by C.R. Bard, Inc
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K212588 |
08/16/2021 |
Conquest 40 PTA Dilatation Catheter, Atlas Gold PTA Dilatation Catheter, Vida PTV Dilatation Catheter, Vida BAV Balloon Valvuloplasty Catheter |
C.R. Bard, Inc |
| K151985 |
07/17/2015 |
PowerPICC« EtOH Catheter and PowerPICC SOLO«2 EtOH Catheter |
C.R. Bard, Inc |
| K162441 |
08/31/2016 |
PowerPICC Provena Catheters with SOLO Valve Technology |
C.R. BARD, INC |
| K153393 |
11/24/2015 |
PowerMidline Catheter |
C.R. BARD, INC |
| K161183 |
04/27/2016 |
Halo One Thin-Walled Guiding Sheath |
C.R. BARD, INC |
| K142443 |
09/02/2014 |
Site-Rite 6 Ultrasound System with Pinpoint GT Technology |
C.R. Bard, Inc |
| K143208 |
11/10/2014 |
Denali Filter System - Femoral Delivery Kit, Denali Filter System - Jugular/Subclavain Delivery Kit |
C.R. Bard, Inc |
| K191232 |
05/08/2019 |
AccuCath Ace Intravascular Catheter |
C.R. Bard, Inc |
| K172511 |
08/21/2017 |
Hickman TriFusion Catheter |
C.R. Bard, Inc |
| K150529 |
03/02/2015 |
Site-Rite Prevue Ultrasound System, Site-Rite Prevue+ Ultrasound System |
C.R. Bard, Inc |
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