FDA 510(k) Applications Submitted by SUSAN SILAVIN, PH.D.

FDA 510(k) Number Submission Date Device Name Applicant
K980119 01/13/1998 ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE GUIDANT CORP.
K982876 08/14/1998 HI-TORQUE STEELCORE 18 GUIDE WIRE MODEL NUMBERS 1003280, 1003281, 1003282 GUIDANT CORP.
K983055 09/01/1998 RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, MODEL #'S 1003006-20, 1003007-20, 1003008-20, 1003009-20, 1003010-20, 1003 GUIDANT CORP.
K993639 10/28/1999 RX VIATRAC 18 PERIPHERAL DILATATION CATHETER, OTW VIATRAC 18 PERIPHERAL DILATATION CATHETER GUIDANT CORP.
K002143 07/17/2000 DYNALINK BILIARY SELF-EXPANDING STENT SYSTEM GUIDANT CORP.


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