510(k) K243830 ยท FAD Stent, Ureteral
Disposable ureteral stent
| Applicant | Shenzhen Trious Medical Technology Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, May 14, 2025 |
| Received | Dec 13, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243830
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.