K-number	K070298
Device name	MODIFICATION TO PALOMAR LUXIR HANDPIECE
Applicant	Palomar Medical Technologies, Inc.
Product code	GEX
Device class	Class II
Decision date	Jul 3, 2007
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO PALOMAR LUXIR HANDPIECE

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