510(k) K173727 ยท EOQ Bronchoscope (Flexible Or Rigid)
Ambu aScope 3 Slim 3.8/1.2 and Ambu aScope 4 Broncho Slim 3.8/1.2; Ambu aScope 3 Regular 5.0/2.2 and Ambu aScope 4 Broncho Regular 5.0/2.2; Ambu aScope 3 Large 5.8/2.8 and Ambu aScope 4 Broncho Large 5.8/2.8; Ambu aView Monitor
| Applicant | Ambu A/S, Ballerup, DK |
| Decision | Substantially Equivalent, Mar 28, 2018 |
| Received | Dec 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173727
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.