K243830
- 510(k) number
- K243830
- Device name
- Disposable ureteral stent
- Applicant
- Shenzhen Trious Medical Technology Co., Ltd. CN
- Product code
- FAD — Stent, Ureteral
- Decision date
- 2025-05-14
- Date received
- 2024-12-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K243830.pdf
Official FDA record: K243830
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.