510(k) K223643 · QRL Multiple Use Blood Lancet For Single Patient Use Only
Verifine® Ease Lancing Device, Verifine® Lancing Device
| Applicant | Promisemed Hangzhou Meditech Co., Ltd., Hangzhou City, CN |
| Decision | Substantially Equivalent, Feb 21, 2023 |
| Received | Dec 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223643
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.