510(k) K211347 ยท FGB Ureteroscope And Accessories, Flexible/Rigid
Uretero1 Ureteroscope System
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Nov 23, 2021 |
| Received | May 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211347
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.