K-number	K160349
Device name	Electronic Sphygmomanometer
Applicant	Guangdong Biolight Meditech Co., Ltd.
Product code	DXN
Device class	Class II
Decision date	Nov 3, 2016
Decision	Substantially Equivalent
Regulation	870.1130

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View the full FDA submission: accessdata.fda.gov

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Electronic Sphygmomanometer

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