510(k) K231261 ยท FMI Needle, Hypodermic, Single Lumen
Altaviz Needle Kit II
| Applicant | Altaviz, LLC, Irvine CA, US |
| Decision | Substantially Equivalent, Jul 27, 2023 |
| Received | May 1, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231261
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.