K-number	K133895
Device name	DEKA SMARTXIDE LASER SYSTEM
Applicant	El.En S.P.A.
Product code	GEX
Device class	Class II
Decision date	Sep 5, 2014
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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DEKA SMARTXIDE LASER SYSTEM

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