FDA 510(k) Applications for Medical Device Product Code "NHW"
(Electrode, Pacing And Cardioversion, Temporary, Epicardial)

FDA 510(k) Number Applicant Device Name Decision Date
K024071 GUIDANT CORPORATION, CARDIAC SURGERY GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM 02/14/2003
K020701 GUIDANT CORPORATION, CARDIAC SURGERY SYNCRUS INTERNAL CARDIOVERSION SYSTEM 05/24/2002


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