K-number	K130294
Device name	BRAEMAR CARDIOKEY HOLTER RECORDER
Applicant	Braemar Manufacturing, LLC
Product code	MWJ
Device class	Class II
Decision date	Oct 16, 2013
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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BRAEMAR CARDIOKEY HOLTER RECORDER

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