510(k) K221072 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
TRUEdraw Lancing Device, Mini Lancing Device
| Applicant | Trividia Health, Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Oct 18, 2022 |
| Received | Apr 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221072
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.