FDA 510(k) Applications Submitted by KAREN S ALSOP
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K021282 |
04/18/2002 |
LV-1 HEMOSTASIS VALVE, MODEL #6789 |
GUIDANT CORP. |
K021283 |
04/18/2002 |
GUIDANT BALLOON CATHETER, SEVERAL MODELS |
GUIDANT CORP. |
K021284 |
04/18/2002 |
EASYTRAK GUIDING CATHETER |
GUIDANT CORP. |
K021285 |
04/18/2002 |
HI-TORQUE EXTRA S'PORT GUIDEWIRE |
GUIDANT CORP. |
K021455 |
05/06/2002 |
RAPIDO GUIDING CATHETER, 6F MODEL# 6776; RAPIDO GUIDING CATHETER, 8F MODEL# 6775, 6777, 6778, 6779, 6780, 6781, 6782, |
GUIDANT CORP. |
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