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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