510(k) K231797 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
Medifun Lancing Device, Model No. LD-E1
| Applicant | Medifun Corporation, Taichung City, TW |
| Decision | Substantially Equivalent, Nov 22, 2023 |
| Received | Jun 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231797
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.