510(k) K212805 ยท FMI Needle, Hypodermic, Single Lumen
SteriCap Mini Needle and Standard Needles
| Applicant | Ocuject, LLC, Newport Beach CA, US |
| Decision | Substantially Equivalent, Sep 30, 2021 |
| Received | Sep 2, 2021 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K212805
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.