510(k) K220603 ยท FMI Needle, Hypodermic, Single Lumen
Disposable Medical Safety Hypodermic Needle
| Applicant | Hantech Medical Device Co., Ltd., Ningbo, CN |
| Decision | Substantially Equivalent, Aug 23, 2022 |
| Received | Mar 2, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220603
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.