ClearanceBrief
510(k) K014206 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

LOGIQBOOK

ApplicantGeneral Electric Co., Milwaukee WI, US
DecisionSubstantially Equivalent, Jan 16, 2002
ReceivedDec 21, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K014206

DateFirm and productCodeLinked 510(k)
Jan 11, 2006General Electric Med Systems LLC
LOCIQ Book System models: 2399921, 2399923, 2349933, 2349934 and 2349935
Terminated
IYNNone listed

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