ClearanceBrief
510(k) K112022 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

DUS-3000/DUS-3000PLUS DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM

ApplicantAdvanced Instrumentations, Inc., Hialeah FL, US
DecisionSubstantially Equivalent, Sep 22, 2011
ReceivedJul 15, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112022

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.