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FDA 510(k) Applications Submitted by STACEY SIMON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K991102
04/01/1999
COPILOT BLEEDBACK CONTROL VALVE, MODEL 1003331
GUIDANT CORP.
K001435
05/08/2000
VIKING OPTIMA GUIDING CATHETER
GUIDANT CORP.
K012002
06/27/2001
VIKING OPTIMA GUIDING CATHETER
GUIDANT CORP.
K994229
12/16/1999
VERIPATH PERIPHERAL GUIDING CATHETER
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
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