510(k) K223700 · MXK Device, Analysis, Anterior Segment
BOSS
| Applicant | Intelon Optics, Inc., Woburn MA, US |
| Decision | Substantially Equivalent, Aug 16, 2024 |
| Received | Dec 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223700
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.