K-number	K982975
Device name	DIGITAL ECG HOLTER RECORDER, MODEL DR512
Applicant	Datrix
Product code	MWJ
Device class	Class II
Decision date	Nov 10, 1998
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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DIGITAL ECG HOLTER RECORDER, MODEL DR512

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