Last synced on 14 November 2025 at 11:06 pm

SOLIX

Page Type
Cleared 510(K)
510(k) Number
K222166
510(k) Type
Traditional
Applicant
Optovue, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2022
Days to Decision
111 days
Submission Type
Summary

SOLIX

Page Type
Cleared 510(K)
510(k) Number
K222166
510(k) Type
Traditional
Applicant
Optovue, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/9/2022
Days to Decision
111 days
Submission Type
Summary