ClearanceBrief
510(k) K081919 ยท ITX Transducer, Ultrasonic, Diagnostic

UF-870 AG DIAGNOSTIC ULTRASOUND SYSTEM

ApplicantFukuda Denshi Co., Ltd., Redmond WA, US
DecisionSubstantially Equivalent, Sep 9, 2008
ReceivedJul 7, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081919

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.