510(k) K230959 · FMI Needle, Hypodermic, Single Lumen
VitreJect® Needle; OcuSafe® Needle
| Applicant | Ocuject, LLC, Newport Beach CA, US |
| Decision | Substantially Equivalent, Sep 14, 2023 |
| Received | Apr 4, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230959
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.