510(k) K182051 ยท FDT Duodenoscope And Accessories, Flexible/Rigid
FUJIFILM Duodenoscope Model
| Applicant | Fujifilm Corporation, Ashigara Kami-Gun, JP |
| Decision | Substantially Equivalent, Oct 2, 2018 |
| Received | Jul 31, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K182051
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.