Last synced on 9 May 2025 at 11:05 pm

R:GEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220974
510(k) Type
Traditional
Applicant
Lutronic Vision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2022
Days to Decision
267 days
Submission Type
Summary

R:GEN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220974
510(k) Type
Traditional
Applicant
Lutronic Vision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2022
Days to Decision
267 days
Submission Type
Summary