510(k) K211332 ยท FET Endoscopic Video Imaging System/Component, Gastroenterology-Urology
D Camera Controller
| Applicant | Richard Wolf Medical Instruments Corporation, Vernon Hills IL, US |
| Decision | Substantially Equivalent, Oct 1, 2021 |
| Received | May 3, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211332
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.