K-number	K133014
Device name	DMS 300-2W HOLTER ECG RECORDER
Applicant	Diagnostic Monitoring Software
Product code	MWJ
Device class	Class II
Decision date	May 19, 2014
Decision	Substantially Equivalent
Regulation	870.2800

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Source

View the full FDA submission: accessdata.fda.gov

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DMS 300-2W HOLTER ECG RECORDER

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