510(k) K221062 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
RIGHTEST Lancing Device GD500, GE Lancing Device, iGlucose Lancing Device
| Applicant | Bionime Corporation, Taichung City, TW |
| Decision | Substantially Equivalent, Sep 26, 2022 |
| Received | Apr 11, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221062
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.