Last synced on 30 May 2025 at 11:05 pm

Myopia Master

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202989
510(k) Type
Traditional
Applicant
OCULUS Optikgeräte GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/14/2021
Days to Decision
287 days
Submission Type
Summary

Myopia Master

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202989
510(k) Type
Traditional
Applicant
OCULUS Optikgeräte GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
7/14/2021
Days to Decision
287 days
Submission Type
Summary