510(k) K222739 ยท FMI Needle, Hypodermic, Single Lumen
Disposable Insulin Pen Needle
| Applicant | Hantech Medical Device Co., Ltd., Ningbo, CN |
| Decision | Substantially Equivalent, Apr 6, 2023 |
| Received | Sep 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222739
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.