ClearanceBrief
510(k) K000571 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

GE LOGIQ 700

ApplicantGE Medical Systems, Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 18, 2000
ReceivedFeb 22, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K000571

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.