FDA 510(k) Applications Submitted by MARTINE D SCHNEIDER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K955886 |
12/28/1995 |
MEGA PTA BALLOON CATHETER |
CORDIS CORP. |
| K970299 |
01/27/1997 |
JUPITER PTA CATHETERS (VARIOUS) |
CORDIS CORP. |
| K030558 |
02/21/2003 |
MAMMOSITE RADIATION THERAPY SYSTEM (RTS) TRAY, MAMMOSITE HDR AFTERLOADER ACCESSORIES TRAY |
PROXIMA THERAPEUTICS, INC. |
| K011690 |
05/31/2001 |
MAMMOSITE RADIATION THERAPY SYSTEM (RTS) TRAY, MAMMOSITE HDR AFTERLOADER ACCESSORIES TRAY |
PROXIMA THERAPEUTICS, INC. |
| K032067 |
07/03/2003 |
MAMMOSITE RADIATION THERAPY SYSTEM (RTS) TRAY, MAMMOSITE HDR AFTERLOADER ACCESSORIES TRAY |
PROXIMA THERAPEUTICS, INC. |
| K041929 |
07/19/2004 |
MAMMOSITE II RADIATION THERAPY SYSTEM (RTS) TRAY, MAMMOSITE HDR AFTERLOADER ACCESSORIES TRAY |
PROXIMA THERAPEUTICS, INC. |
| K982632 |
07/23/1998 |
ENVOY AND VISTA BRITE TIP |
CORDIS CORP. |
| K982770 |
07/23/1998 |
6F ENVOY GUIDING CATHETER |
CORDIS CORP. |
| K983003 |
08/28/1998 |
1 MASS TRANSIT INFUSION CATHETER, 1 VARIOUS |
CORDIS NEUROVASCULAR, INC. |
| K983483 |
10/05/1998 |
VASCULAR OCCLUSION SYSTEM |
CORDIS NEUROVASCULAR, INC. |
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