K-number	K121224
Device name	GENESIS HEALTH TECHNOLOGIES BLOOD GLUCOSE MONITORING SYSTEM
Applicant	Taidoc Technology Corporation
Product code	LFR
Device class	Class II
Decision date	Sep 19, 2012
Decision	Substantially Equivalent
Regulation	862.1345

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View the full FDA submission: accessdata.fda.gov

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GENESIS HEALTH TECHNOLOGIES BLOOD GLUCOSE MONITORING SYSTEM

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