K-number	K091497
Device name	K-LASER K-1200, MODEL 12 W
Applicant	Eltech S.R.L
Product code	ILY
Device class	Class II
Decision date	Aug 19, 2009
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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K-LASER K-1200, MODEL 12 W

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