K-number	K162042
Device name	OptiScanner 5000 Glucose Monitoring System
Applicant	Optiscan Biomedical Corp.
Product code	LZF
Device class	Class II
Decision date	Oct 16, 2017
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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OptiScanner 5000 Glucose Monitoring System

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