510(k) K183188 ยท FGB Ureteroscope And Accessories, Flexible/Rigid
Flexible Sensor-Ureterorenoscopes BOA Vision EF, Flexible Sensor-Ureterorenoscopes COBRA Vision EF
| Applicant | Richard Wolf Medical Instruments Corporation, Vernon Hills IL, US |
| Decision | Substantially Equivalent, May 3, 2019 |
| Received | Nov 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183188
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.