FDA 510(k) Applications Submitted by MIKE BURNSIDE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080806 |
03/21/2008 |
ANGIOJET ULTRA SPIROFLEX VG THROMBECTOMY SET, MODEL 106608 |
POSSIS MEDICAL, INC. |
| K051096 |
04/29/2005 |
APEEL CS PLUS CATHETER DELIVERY SYSTEM, MODELS 407579, 407580, 407581, 407582 |
ST. JUDE MEDICAL, DAIG DIVISION, INC. |
| K081454 |
05/23/2008 |
GUARDDOG OCCLUSION GUIDEWIRE, INFLATION DEVICE |
POSSIS MEDICAL, INC. |
| K031906 |
06/20/2003 |
APEEL CS CATHETER DELIVERY SYSTEM |
ST. JUDE MEDICAL |
| K081989 |
07/14/2008 |
MODIFICATION TO FETCH ASPIRATION CATHETER |
POSSIS MEDICAL, INC. |
| K112086 |
07/21/2011 |
MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM / TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION SYRINGE |
MEDRAD, INC. |
| K072269 |
08/15/2007 |
ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL: 106552 |
POSSIS MEDICAL, INC. |
| K072769 |
09/28/2007 |
ANGIOJET ULTRA; XMI (105041), XVG (105042) AND SPIROFLEX (106553) THROMBECTOMY SETS |
POSSIS MEDICAL, INC. |
| K113133 |
10/24/2011 |
MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM), (TABLE MOUNT SYSTEM), MEDRAD MARK 7 ARTERION ARTERION SYRINGE |
MEDRAD, INC. |
| K113363 |
11/15/2011 |
ANGIOJET SOLENT DISTA THROMBECTOMY SET |
MEDRAD, INC. |
| K113428 |
11/21/2011 |
ANGIOJET ULTRA DVX THROMBECTOMY SET |
MEDRAD, INC. |
| K073441 |
12/07/2007 |
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 |
POSSIS MEDICAL, INC. |
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