K-number	K152626
Device name	H3+ Holter Recorder
Applicant	Mortara Instrument, Inc.
Product code	MWJ
Device class	Class II
Decision date	Feb 26, 2016
Decision	Substantially Equivalent
Regulation	870.2800

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Source

View the full FDA submission: accessdata.fda.gov

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H3+ Holter Recorder

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