Lancet— 510(k) K262211
Substantially EquivalentTianjin Huahong Technology Co., Ltd.
FDA 510(k) clearance K262211 for Lancet, Substantially Equivalent on 2026-07-22. Applicant: Tianjin Huahong Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Tianjin Huahong Technology Co., Ltd.
- Product code
- Code QRL
- Device class
- Class 2
- Regulation
- 21 CFR 878.4850
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Tianjin, CN
Recent devices under product code QRL
view all- K260122 — Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)
- K253706 — Lancing device (HH-XV-T)
- K250813 — MICROLET®NEXT 2 Lancing Device
- K243306 — 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)
- K232912 — Facet Aurora Reusable Lancet Base
More clearances from Tianjin Huahong Technology Co., Ltd.
view allAdverse events under product code QRL
product code QRL- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.