FDA 510(k) Applications Submitted by GUIDANT CORPORATION, CARDIAC SURGERY

FDA 510(k) Number Submission Date Device Name Applicant
K023629 10/28/2002 ESSEX DISSECTION CANNULA, MODEL SXD-1100, ESSEX DISSECTION TIP, MODEL SXD-1200 GUIDANT CORPORATION, CARDIAC SURGERY
K020143 01/16/2002 VASOVIEW 5 HARVESTING CANNULA GUIDANT CORPORATION, CARDIAC SURGERY
K022718 08/15/2002 VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002 GUIDANT CORPORATION, CARDIAC SURGERY
K020701 03/04/2002 SYNCRUS INTERNAL CARDIOVERSION SYSTEM GUIDANT CORPORATION, CARDIAC SURGERY
K024071 12/10/2002 GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM GUIDANT CORPORATION, CARDIAC SURGERY
K080169 01/24/2008 HEARTSTRING III PROXIMAL SEAL SYSTEM GUIDANT CORPORATION, CARDIAC SURGERY
K041340 05/20/2004 GUIDANT MICROWAVE ABLATION SYSTEM GUIDANT CORPORATION, CARDIAC SURGERY
K023630 10/28/2002 ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400 GUIDANT CORPORATION, CARDIAC SURGERY


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