510(k) K232920 · FAD Stent, Ureteral
RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cm
| Applicant | Ureteral Stent Company, Chagrin Falls OH, US |
| Decision | Substantially Equivalent, Mar 22, 2024 |
| Received | Sep 19, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232920
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.