K-number	K103179
Device name	PRELUDE II TOUNGE SUSPENSION SYSTEM
Applicant	Siesta Medical, Inc.
Product code	ORY
Device class	Class II
Decision date	Dec 20, 2010
Decision	Substantially Equivalent
Regulation	872.5570

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View the full FDA submission: accessdata.fda.gov

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PRELUDE II TOUNGE SUSPENSION SYSTEM

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