K-number	K991284
Device name	ANTERIOR EYE-SEGMENT ANALYSIS SYSTEM
Applicant	Nidek, Inc.
Product code	MXK
Device class	Class II
Decision date	Aug 6, 1999
Decision	Substantially Equivalent
Regulation	886.1850

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View the full FDA submission: accessdata.fda.gov

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ANTERIOR EYE-SEGMENT ANALYSIS SYSTEM

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