K253706
- 510(k) number
- K253706
- Device name
- Lancing device (HH-XV-T)
- Applicant
- Tianjin Huahong Technology Co., Ltd. CN
- Product code
- QRL — Multiple Use Blood Lancet For Single Patient Use Onl
- Decision date
- 2025-12-09
- Date received
- 2025-11-24
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K253706.pdf
Official FDA record: K253706
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.