510(k) K221419 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
TD-5010 Lancing Device and TD-5084 Sterile Lancets
| Applicant | Gostar Co., Ltd., New Taipei City, TW |
| Decision | Substantially Equivalent, Jan 20, 2023 |
| Received | May 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221419
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.