Last synced on 16 May 2025 at 11:05 pm

ME-APDS™; MAGENTIQ-COLO™

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223473
510(k) Type
Traditional
Applicant
Magentiq Eye LTD
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/25/2023
Days to Decision
250 days
Submission Type
Summary

ME-APDS™; MAGENTIQ-COLO™

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223473
510(k) Type
Traditional
Applicant
Magentiq Eye LTD
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/25/2023
Days to Decision
250 days
Submission Type
Summary