510(k) K183016 ยท FMI Needle, Hypodermic, Single Lumen
SteriCap Mini Needle
| Applicant | Ocujet, LLC, Newport Beach CA, US |
| Decision | Substantially Equivalent, May 7, 2019 |
| Received | Oct 31, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K183016
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.