K-number	K011723
Device name	ANTI-SNORING DEVICE OR ASD
Applicant	Pi Medical
Product code	LRK
Device class	Class II
Decision date	Dec 18, 2002
Decision	Substantially Equivalent
Regulation	872.5570

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Source

View the full FDA submission: accessdata.fda.gov

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ANTI-SNORING DEVICE OR ASD

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