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RTVue XR OCT Avanti with AngioVue Software

Page Type
Cleared 510(K)
510(k) Number
K153080
510(k) Type
Traditional
Applicant
Optovue, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2016
Days to Decision
111 days
Submission Type
Summary

RTVue XR OCT Avanti with AngioVue Software

Page Type
Cleared 510(K)
510(k) Number
K153080
510(k) Type
Traditional
Applicant
Optovue, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/11/2016
Days to Decision
111 days
Submission Type
Summary