K-number	K192785
Device name	OptiScanner® 5000 Glucose Monitoring System
Applicant	Optiscan Biomedical Corporation
Product code	LZF
Device class	Class II
Decision date	Feb 5, 2020
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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