510(k) K222933 ยท MXK Device, Analysis, Anterior Segment
MYAH
| Applicant | Visia Imaging S.R.L., San Giovanni Valdarno, IT |
| Decision | Substantially Equivalent, Jun 29, 2023 |
| Received | Sep 26, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222933
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.