K-number	K133862
Device name	ACCU-CHEK AVIVA PLUS SYSTEM
Applicant	Roche Diagnostics Corporation
Product code	NBW
Device class	Class II
Decision date	Apr 29, 2014
Decision	Substantially Equivalent
Regulation	862.1345

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View the full FDA submission: accessdata.fda.gov

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ACCU-CHEK AVIVA PLUS SYSTEM

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