510(k) K233671 · EOQ Bronchoscope (Flexible Or Rigid)
Ambu® aScope 5 Broncho 4.2/2.2; Ambu® aScope 5 Broncho 2.7/1.2; Ambu® aView 2 Advance
| Applicant | Ambu A/S, Ballerup, DK |
| Decision | Substantially Equivalent, Jan 4, 2024 |
| Received | Nov 15, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K233671
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.