K-number	K951760
Device name	OPTILITE VIII LASER SURGERY ACCESSORIES
Applicant	Xintec Corporation
Product code	GEX
Device class	Class II
Decision date	Nov 29, 1995
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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OPTILITE VIII LASER SURGERY ACCESSORIES

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