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FDA 510(k), K024071, GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM
FDA 510(k), K024071, GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM
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$149.00 USD
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$149.00 USD
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510(K) Number: K024071
Device Name: GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM
Manufacturer:
Device Classification Name: Electrode, Pacing And Cardioversion, Temporary, Epicardial
Regulation Number: 870.3680
Classification Product Code: NHW
Date Received: 12/10/2002
Decision Date: 02/14/2003
Regulation Medical Specialty: Cardiovascular
Device Name: GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM
Manufacturer:
Device Classification Name: Electrode, Pacing And Cardioversion, Temporary, Epicardial
Regulation Number: 870.3680
Classification Product Code: NHW
Date Received: 12/10/2002
Decision Date: 02/14/2003
Regulation Medical Specialty: Cardiovascular
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