K-number	K131366
Device name	ACCU-CHEK AVIVA EXPERT BLOOD GLUCOSE MONITORING SYSTEM
Applicant	Roche Diagnostics Operations, Inc.
Product code	LFR
Device class	Class II
Decision date	Oct 11, 2013
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 EXPERT BLOOD GLUCOSE MONITORING SYSTEM

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