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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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