K-number	K153080
Device name	RTVue XR OCT Avanti with AngioVue Software
Applicant	Optovue, Inc.
Product code	HLI
Device class	Class II
Decision date	Feb 11, 2016
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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RTVue XR OCT Avanti with AngioVue Software

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