K-number	K071937
Device name	BONALIVE GRANULES AND BONALIVE PLATES
Applicant	Vivoxid , Ltd.
Product code	KKY
Device class	Class II
Decision date	Oct 19, 2007
Decision	Substantially Equivalent
Regulation	878.3500

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View the full FDA submission: accessdata.fda.gov

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BONALIVE GRANULES AND BONALIVE PLATES

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