K-number	K894273
Device name	NIDEK MODEL AKC-8000
Applicant	Nidek, Inc.
Product code	HQF
Device class	Class II
Decision date	Aug 7, 1989
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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NIDEK MODEL AKC-8000

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