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FDA 510(k) Applications Submitted by MICHELLE GROSSMAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032530
08/15/2003
MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM
GUIDANT CORPORATION
K072708
09/25/2007
ABSOLUTE PRO .035 SELF-EXPANDING STENT SYSTEM
ABBOTT VASCULAR-VASCULAR SOLUTIONS
K023320
10/04/2002
AGILTRAC .035 PERIPHERAL DILATATION CATHETER
GUIDANT CORP.
K033834
12/10/2003
OMNILINK .018 BILIARY STENT SYSTEM
GUIDANT CORP.
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