Last synced on 30 May 2025 at 11:05 pm

SOLIX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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