RTVue XR OCT Avanti with AngioVue Software— 510(k) K153080

Substantially Equivalent

Optovue, Inc.

FDA 510(k) clearance K153080 for RTVue XR OCT Avanti with AngioVue Software, Substantially Equivalent on 2016-02-11. Applicant: Optovue, Inc..

Clearance details

Applicant: Optovue, Inc.
Product code: Code HLI
Advisory panel: Ophthalmic
Date received: 2015-10-23
Decision date: 2016-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fremont, CA, US

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