510(k) K202989 · MXK Device, Analysis, Anterior Segment
Myopia Master
| Applicant | Oculus Optikgeräte GmbH, Wetzlar, DE |
| Decision | Substantially Equivalent, Jul 14, 2021 |
| Received | Sep 30, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K202989
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 30, 2023 | Oculus Optikgeraete GMBH Oculus Myopia Master , Ref 68100, CE 0123 Open, Classified |
MXK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.