K243306
- 510(k) number
- K243306
- Device name
- 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. CN
- Product code
- QRL — Multiple Use Blood Lancet For Single Patient Use Onl
- Decision date
- 2024-11-15
- Date received
- 2024-10-21
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K243306.pdf
Official FDA record: K243306
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.