510(k) K220370 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)
| Applicant | Tianjin Huahong Technology Co., Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, May 19, 2022 |
| Received | Feb 9, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220370
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.