FDA 510(k) Applications Submitted by AARON CONOVALOFF
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K220270 |
01/31/2022 |
Aspirex Thrombectomy System |
C.R. Bard, Inc. |
| K230356 |
02/09/2023 |
AspirexÖ Thrombectomy System |
C.R. Bard, Inc. |
| K150667 |
03/16/2015 |
True Dilatation Balloon Valvuloplasty Catheter |
C.R. Bard, Inc. |
| K131002 |
04/10/2013 |
VIDA PTV DILATATON CATHETER |
C.R. BARD, INC. |
| K181323 |
05/18/2018 |
Atlas Gold PTA Dilatation Catheter |
C. R. Bard, Inc. |
| K211738 |
06/07/2021 |
Rotarex Atherectomy System |
C.R. Bard, Inc. |
| K141985 |
07/22/2014 |
TRUE BA V BALLOON VALVULOPLASTY CATHETER |
C.R. BARD, INC. |
| K142083 |
07/31/2014 |
TRUE FLOW VALVULOPLASTY PERFUSION 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. |
| K203363 |
11/16/2020 |
Crosser iQ CTO Recanalization System |
C.R. Bard, Inc. |
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