510(k) K262135 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
Lancing device
| Applicant | Tianjin Huahong Technology Co., Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Aug 18, 2026 |
| Received | Jun 25, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K262135
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.