510(k) K172095 ยท FMI Needle, Hypodermic, Single Lumen
Autokeeper
| Applicant | Medexel Co.,Ltd, Anseong-Si, KR |
| Decision | Substantially Equivalent, Jul 24, 2018 |
| Received | Jul 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172095
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.