K-number	K090195
Device name	PALOMAR LUX1540 HANDPIECE
Applicant	Palomar Medical Technologies, Inc.
Product code	GEX
Device class	Class II
Decision date	Nov 20, 2009
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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PALOMAR LUX1540 HANDPIECE

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