510(k) K201098 ยท FDT Duodenoscope And Accessories, Flexible/Rigid
Ambu Duodeno System
| Applicant | Ambu Innovation GmbH, Kissing, DE |
| Decision | Substantially Equivalent, Jul 17, 2020 |
| Received | Apr 24, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201098
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.