510(k) K243039 ยท FAD Stent, Ureteral
Ureteral Stents (AF-D series)
| Applicant | Alton (Shanghai) Medical Instruments Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Jun 18, 2025 |
| Received | Sep 27, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243039
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.