K-number	K101024
Device name	KENZ CARDY302 MAX
Applicant	Suzuken Co., Ltd.
Product code	MWJ
Device class	Class II
Decision date	Jan 6, 2011
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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KENZ CARDY302 MAX

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