ClearanceBrief
510(k) K242108 · FGB Ureteroscope And Accessories, Flexible/Rigid

Ambu® aScope™ 5 Uretero (Standard Deflection); Ambu® aScope™ 5 Uretero (Reverse Deflection); Ambu® aView™ 2 Advance

ApplicantAmbu A/S, Ballerup, DK
DecisionSubstantially Equivalent, Aug 16, 2024
ReceivedJul 18, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K242108

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.