K-number	K101709
Device name	LAMBERGSLEEPWELL- SMARTRUSION (LSW-S)
Applicant	Steven B. Lamberg, Dds
Product code	LRK
Device class	Class II
Decision date	Aug 18, 2010
Decision	Substantially Equivalent
Regulation	872.5570

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View the full FDA submission: accessdata.fda.gov

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LAMBERGSLEEPWELL- SMARTRUSION (LSW-S)

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