ClearanceBrief
510(k) K180970 ยท ITX Transducer, Ultrasonic, Diagnostic

Disposable guides KDNG00

ApplicantKoelis, Meylan, FR
DecisionSubstantially Equivalent, Jul 10, 2018
ReceivedApr 13, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180970

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.