FDA 510(k) Applications Submitted by JACQUELINE J JACKSON

FDA 510(k) Number Submission Date Device Name Applicant
K003495 11/13/2000 ANCURE LLIAC BALLOON CATHETER GUIDANT CARDIAC AND VASCULAR SURGERY
K003889 12/18/2000 ANCURE SHEATH MODEL # 40315, 40320, 40325 GUIDANT CARDIAC AND VASCULAR SURGERY


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