K262211
- 510(k) number
- K262211
- Device name
- Lancet
- Applicant
- Tianjin Huahong Technology Co., Ltd. CN
- Product code
- QRL — Multiple Use Blood Lancet For Single Patient Use Onl
- Decision date
- 2026-07-22
- Date received
- 2026-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K262211.pdf
Official FDA record: K262211
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.