K-number	K163696
Device name	SleepImage System
Applicant	Mycardio, LLC Dba Sleepimage.
Product code	MNR
Device class	Class II
Decision date	Oct 13, 2017
Decision	Substantially Equivalent
Regulation	868.2375

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Source

View the full FDA submission: accessdata.fda.gov

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SleepImage System

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