K-number	K130028
Device name	RESURFX 1565NM LASER MODULE
Applicant	Lumenis, Ltd.
Product code	ONG
Device class	Class II
Decision date	Sep 3, 2013
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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RESURFX 1565NM LASER MODULE

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