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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