K-number	K123738
Device name	MARK 5 NUVO LITE OCSI, MARK 5 NUVO LITE STD
Applicant	Nidek Medical Products, Inc.
Product code	CAW
Device class	Class II
Decision date	Feb 28, 2013
Decision	Substantially Equivalent
Regulation	868.5440

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Source

View the full FDA submission: accessdata.fda.gov

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MARK 5 NUVO LITE OCSI, MARK 5 NUVO LITE STD

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