ClearanceBrief
510(k) K072797 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

ApplicantGeneral Electric Co., Wauwatosa WI, US
DecisionSubstantially Equivalent, Oct 17, 2007
ReceivedOct 1, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072797

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.