510(k) K243322 ยท QLY Ophthalmic Syringe
Altaviz Intravitreal Syringe
| Applicant | Altaviz, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, May 9, 2025 |
| Received | Oct 23, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243322
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.