K-number	K092003
Device name	CPC SLEEP DATA RECORDER, MODEL M1, AND APPLICATION SOFTWARE
Applicant	MyCardio, LLC
Product code	MNR
Device class	Class II
Decision date	Sep 30, 2009
Decision	Substantially Equivalent
Regulation	868.2375

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View the full FDA submission: accessdata.fda.gov

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CPC SLEEP DATA RECORDER, MODEL M1, AND APPLICATION SOFTWARE

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