510(k) K233343 ยท FMI Needle, Hypodermic, Single Lumen
SteriCap Safety Needle; VitreJect Safety Needle
| Applicant | Ocuject, LLC, Newport Beach CA, US |
| Decision | Substantially Equivalent, Nov 27, 2023 |
| Received | Sep 29, 2023 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K233343
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.