ClearanceBrief
510(k) K220606 ยท EOQ Bronchoscope (Flexible Or Rigid)

Ambu aScope 5 Broncho HD 5.6/2.8, Ambu aScope 5 Broncho HD 5.0/2.2, Ambu aBox 2

ApplicantAmbu A/S, Ballerup, DK
DecisionSubstantially Equivalent, Jul 25, 2022
ReceivedMar 2, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220606

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.