K-number	K861063
Device name	NIDEK KM-800 AUTO KERATOMETER
Applicant	Nidek, Inc.
Product code	HLQ
Device class	Class I
Decision date	Apr 4, 1986
Decision	Substantially Equivalent
Regulation	886.1350

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View the full FDA submission: accessdata.fda.gov

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NIDEK KM-800 AUTO KERATOMETER

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