510(k) K233886 · FDT Duodenoscope And Accessories, Flexible/Rigid
Ambu® aScope Duodeno 2, Ambu® aBox 2
| Applicant | Ambu A/S, Ballerup, DK |
| Decision | Substantially Equivalent, Apr 16, 2024 |
| Received | Dec 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233886
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.