ClearanceBrief
510(k) K161787 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

ACUSON NX2 Diagnostic Ultrasound Systems

ApplicantSiemens Medical Solutions USA, Inc., Moutain View CA, US
DecisionSubstantially Equivalent, Jul 28, 2016
ReceivedJun 29, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K161787

DateFirm and productCodeLinked 510(k)
Jan 28, 2019Siemens Medical Solutions USA, Inc.
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11B; UDI # 04056869030005 The ACUSON NX2 diagnostic
Open, Classified
IYNNone listed

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