K260122
- 510(k) number
- K260122
- Device name
- Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)
- Applicant
- SteriLance Medical (Suzhou), Inc. CN
- Product code
- QRL — Multiple Use Blood Lancet For Single Patient Use Onl
- Decision date
- 2026-07-06
- Date received
- 2026-01-15
- 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: K260122.pdf
Official FDA record: K260122
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.