K-number	K142089
Device name	ACCU-CHEK AVIVA EXPERT SYSTEM
Applicant	Roche Diagnostics Corporation
Product code	LFR
Device class	Class II
Decision date	Dec 17, 2014
Decision	Substantially Equivalent
Regulation	862.1345

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Source

View the full FDA submission: accessdata.fda.gov

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ACCU-CHEK AVIVA EXPERT SYSTEM

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