ClearanceBrief
510(k) K092079 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

MODIFICATION TO GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND

ApplicantGe Medical Systems Israel, Ultrasound, Ltd., Waukesha WI, US
DecisionSubstantially Equivalent, Aug 6, 2009
ReceivedJul 9, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K092079

DateFirm and productCodeLinked 510(k)
Dec 22, 2022GE Medical Systems, LLC
Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult
Open, Classified
IYNNone listed
Dec 22, 2022GE Medical Systems, LLC
Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult
Open, Classified
IYNNone listed

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