K-number	K003299
Device name	OPD-SCAN, MODELS ARK-10000 AND ARK-9000
Applicant	Nidek Co., Ltd.
Product code	HLQ
Device class	Class I
Decision date	Mar 9, 2001
Decision	Unknown
Regulation	886.1350

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View the full FDA submission: accessdata.fda.gov

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OPD-SCAN, MODELS ARK-10000 AND ARK-9000

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