510(k) K243306 ยท QRL Multiple Use Blood Lancet For Single Patient Use Only
Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing device (HH-X-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, HH-XXV-T, HH-XXVI-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XIII-T, HH-XXVII-T)
| Applicant | Tianjin Huahong Technology Co., Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Nov 15, 2024 |
| Received | Oct 21, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K243306
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.