K-number	K131858
Device name	DIGITAL ELECTROCARDIOGRAPH
Applicant	Guangdong Biolight Meditech Co., Ltd.
Product code	DPS
Device class	Class II
Decision date	Jun 11, 2014
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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DIGITAL ELECTROCARDIOGRAPH

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