K-number	K001211
Device name	MODIFICATION TO INTRALASE 600C LASER KERATOME
Applicant	Intra Lase Corp.
Product code	GEX
Device class	Class II
Decision date	Dec 4, 2000
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO INTRALASE 600C LASER KERATOME

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