K-number	K121739
Device name	IVUE WITH NORMATIVE DATABASE
Applicant	Optovue, Inc.
Product code	HLI
Device class	Class II
Decision date	Jan 18, 2013
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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IVUE WITH NORMATIVE DATABASE

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