FDA 510(k) Applications Submitted by MARK D STENOIEN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040013 |
01/05/2004 |
ANGIOJET XPEEDIOR 120 CATHETER AND ANGIOJET POWER PULSE SPRAY ANCILLARY KIT |
POSSIS MEDICAL, INC. |
| K050794 |
03/29/2005 |
ANGIOJET DVX RHEOLYTIC THROMBECTOMY CATHETER |
POSSIS MEDICAL, INC. |
| K031357 |
04/30/2003 |
GUARDDOG OCCLUSION SYSTEM, OCCLUSION GUIDEWIRE, 300 CM, GUARDDOG OCCLUSION SYSTEM OCCLUSION GUIDEWIRE, 200 CM |
POSSIS MEDICAL, INC. |
| K071342 |
05/14/2007 |
ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040, 105042, 106552, 105043, 105041, 106553, 105039 |
POSSIS MEDICAL, INC. |
| K052256 |
08/18/2005 |
ANGIOJET XPEEDIOR 120 CATHETER |
POSSIS MEDICAL, INC. |
| K082382 |
08/19/2008 |
ANGIOJET ULTRA AVX THROMBECTOMY SET, MODEL 105039 |
POSSIS MEDICAL, INC. |
| K042874 |
10/18/2004 |
ANGIOJET XMI CATHETER - RAPID EXCHANGE (XMI-RX) |
POSSIS MEDICAL, INC. |
| K062220 |
08/02/2006 |
MODIFICATION TO GUARDDOG OCCLUSION SYSTEM |
POSSIS MEDICAL, INC. |
|
|
