ClearanceBrief
510(k) K014097 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

GE LOGIQ 5

ApplicantGE Medical Systems, Milwaukee WI, US
DecisionSubstantially Equivalent, Jan 10, 2002
ReceivedDec 12, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K014097

DateFirm and productCodeLinked 510(k)
Jan 11, 2006General Electric Med Systems LLC
LOGIQ 5 system models 2331752, 2331753, 2332750, 2353313 and 2355477.
Terminated
IYNNone listed

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