K-number	K993153
Device name	INTRALASE 600C LASER KERATOME
Applicant	Intra Lase Corp.
Product code	GEX
Device class	Class II
Decision date	Dec 17, 1999
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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INTRALASE 600C LASER KERATOME

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