K251890
- 510(k) number
- K251890
- Device name
- Disposable Ureteral Stents
- Applicant
- Zhejiang Chuangxiang Medical Technology Co., Ltd. CN
- Product code
- FAD — Stent, Ureteral
- Decision date
- 2026-02-20
- Date received
- 2025-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K251890.pdf
Official FDA record: K251890
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.