510(k) K234081 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
RedDrop ONE (One)
| Applicant | Reddrop DX, Fort Collins CO, US |
| Decision | Unknown, Mar 21, 2024 |
| Received | Dec 22, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K234081
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.