ClearanceBrief
510(k) K260309 · EOQ Bronchoscope (Flexible Or Rigid)

Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler Set

ApplicantAmbu A/S, Ballerup, DK
DecisionSubstantially Equivalent, Sep 16, 2026
ReceivedJan 30, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K260309

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.