510(k) K220475 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
Lancet (I, II, III, V, VI); Lancing device (HH-X-T, HH-XIII-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T)
| Applicant | Tianjin Huahong Technology Co., Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Jul 6, 2022 |
| Received | Feb 18, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220475
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.