K252490
- 510(k) number
- K252490
- Device name
- Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)
- Applicant
- Tianjin Huahong Technology Co., Ltd. CN
- Product code
- FMK — Single Use Only Blood Lancet With An Integral Sharps
- Decision date
- 2026-02-12
- Date received
- 2025-08-08
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252490.pdf
Official FDA record: K252490
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.