ClearanceBrief
510(k) K152309 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

LOGIQ E9, LOGIQ E9 XDClear 2.0

ApplicantGE Medical Systems Ultrasound and Primary Care Diagnostics, Wauwatosa WI, US
DecisionSubstantially Equivalent, Sep 14, 2015
ReceivedAug 14, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K152309

DateFirm and productCodeLinked 510(k)
Jul 12, 2019GE Healthcare, LLC
Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
Terminated
IYNNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.