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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