K241627
- 510(k) number
- K241627
- Device name
- Safety Lancet (XXXV)
- Applicant
- Tianjin Huahong Technology Co., Ltd. CN
- Product code
- FMK — Single Use Only Blood Lancet With An Integral Sharps
- Decision date
- 2024-06-20
- Date received
- 2024-06-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241627.pdf
Official FDA record: K241627
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.