ClearanceBrief
510(k) K223832 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

Vivid S60N, Vivid S70N

ApplicantGe Medical System Ultrasound and Primary Care Diagnostics, Wauwatosa WI, US
DecisionSubstantially Equivalent, Feb 16, 2023
ReceivedDec 22, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223832

DateFirm and productCodeLinked 510(k)
Jul 10, 2023GE Vingmed Ultrasound As
GE Healthcare Vivid S60N, ultrasound device
Open, Classified
IYNNone listed
Jul 10, 2023GE Vingmed Ultrasound As
GE Healthcare Vivid S70N, ultrasound device
Open, Classified
IYNNone listed

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