K244018
- 510(k) number
- K244018
- Device name
- Disposable Biopsy Needle
- Applicant
- Zhejiang Curaway Medical Technology Co., Ltd. CN
- Product code
- KNW — Instrument, Biopsy
- Decision date
- 2025-07-22
- Date received
- 2024-12-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K244018.pdf
Official FDA record: K244018
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.