K-number	K051592
Device name	MODIFICATION TO ACCU-CHEK GO SYSTEM
Applicant	Roche Diagnostics Corp.
Product code	LFR
Device class	Class II
Decision date	Sep 2, 2005
Decision	Substantially Equivalent
Regulation	862.1345

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ACCU-CHEK GO SYSTEM

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