K-number	K122725
Device name	TANDA PEARL, ULTRAWYTE, PEARL
Applicant	Syneron Beauty
Product code	EEG
Device class	Class I
Decision date	Nov 27, 2012
Decision	Substantially Equivalent
Regulation	872.6475

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View the full FDA submission: accessdata.fda.gov

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TANDA PEARL, ULTRAWYTE, PEARL

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