K-number	K142722
Device name	3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200
Applicant	Livetec GmbH
Product code	ILY
Device class	Class II
Decision date	Jan 13, 2015
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200

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