K-number	K020701
Device name	SYNCRUS INTERNAL CARDIOVERSION SYSTEM
Applicant	Guidant Corporation, Cardiac Surgery
Product code	NHW
Device class	Class II
Decision date	May 24, 2002
Decision	Substantially Equivalent
Regulation	870.3680

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View the full FDA submission: accessdata.fda.gov

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SYNCRUS INTERNAL CARDIOVERSION SYSTEM

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