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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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