K-number	K083620
Device name	SOMNOLYZER 24X7
Applicant	The Siesta Group North America
Product code	MNR
Device class	Class II
Decision date	Mar 6, 2009
Decision	Substantially Equivalent
Regulation	868.2375

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View the full FDA submission: accessdata.fda.gov

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SOMNOLYZER 24X7

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