510(k) K220030 ยท MLZ Vitrectomy, Instrument Cutter
Vista Ophthalmics Vitrectomy Probe
| Applicant | Vista Ophthalmics, LLC, Katy TX, US |
| Decision | Substantially Equivalent, May 4, 2022 |
| Received | Jan 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220030
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.