ClearanceBrief
510(k) K001016 ยท ITX Transducer, Ultrasonic, Diagnostic

GE LOGIQ 700

ApplicantGE Medical Systems, Milwaukee WI, US
DecisionSubstantially Equivalent, Apr 24, 2000
ReceivedMar 29, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K001016

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.