510(k) K222417 ยท FMI Needle, Hypodermic, Single Lumen
Shina Safety Needle
| Applicant | Shina Corporation, Gongju, KR |
| Decision | Substantially Equivalent, Mar 20, 2023 |
| Received | Aug 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222417
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.