Last synced on 25 January 2026 at 3:41 am

R T VUE WITH SOFTWARE 5.0 MODEL: R I VUE 100

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100861
510(k) Type
Special
Applicant
Optovue, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2010
Days to Decision
83 days
Submission Type
Summary

R T VUE WITH SOFTWARE 5.0 MODEL: R I VUE 100

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K100861
510(k) Type
Special
Applicant
Optovue, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2010
Days to Decision
83 days
Submission Type
Summary