K-number	K993618
Device name	DXP1000 HOLTER RECORDER
Applicant	Braemar Corp.
Product code	MWJ
Device class	Class II
Decision date	Nov 24, 1999
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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DXP1000 HOLTER RECORDER

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