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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