K-number	K132633
Device name	OKMETER DIRECT BLOOD GLUCOSE MONITORING SYSTEM
Applicant	Ok Biotech Co., Ltd.
Product code	NBW
Device class	Class II
Decision date	Aug 14, 2014
Decision	Substantially Equivalent
Regulation	862.1345

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View the full FDA submission: accessdata.fda.gov

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OKMETER DIRECT BLOOD GLUCOSE MONITORING SYSTEM

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