K251469
- 510(k) number
- K251469
- Device name
- Endura Ureteral Stent and Stent Set
- Applicant
- Cathegenix (Xiamen) Co., Ltd. CN
- Product code
- FAD — Stent, Ureteral
- Decision date
- 2025-12-19
- Date received
- 2025-05-13
- Decision
- Unknown
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251469.pdf
Official FDA record: K251469
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.