510(k) K222055 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Disposable Sterile Lancet
| Applicant | Tianjin Rilifine Medical Device Co., Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Nov 15, 2022 |
| Received | Jul 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222055
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.