K-number	K130538
Device name	WINX SLEEP THERAPY SYSTEM
Applicant	Apnicure, Inc.
Product code	OZR
Device class	Class II
Decision date	May 22, 2013
Decision	Substantially Equivalent
Regulation	872.5570

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Source

View the full FDA submission: accessdata.fda.gov

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WINX SLEEP THERAPY SYSTEM

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