K-number	K111353
Device name	ACCU-CHECK COMBO SYSTEM
Applicant	Roche Diagnostics
Product code	LZG
Device class	Class II
Decision date	Jul 17, 2012
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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ACCU-CHECK COMBO SYSTEM

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