K-number	K932932
Device name	SNOREMASTER SNORE REMEDY
Applicant	The Snoremaster Co.
Product code	LQZ
Device class	Class II
Decision date	Feb 10, 1995
Decision	Substantially Equivalent
Regulation	872.5570

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View the full FDA submission: accessdata.fda.gov

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SNOREMASTER SNORE REMEDY

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