510(k) K024033 ยท FDT Duodenoscope And Accessories, Flexible/Rigid
XTJF-160AF DUODENOVIDEOSCOPE
| Applicant | Olympus Optical Co., Ltd., Melville NY, US |
| Decision | Substantially Equivalent, Dec 20, 2002 |
| Received | Dec 6, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024033
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 15, 2016 | Olympus Corporation of the Americas EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF
used with an Olympus video system center, light source, documentation equipment monitors, Endo Therapy accessories and other ancillary equipment f Terminated |
FDT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.