ClearanceBrief
510(k) K202683 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

ACUSON Sequoia Diagnostic Ultrasound System, ACUSON SC2000 Diagnostic Ultrasound System, ACUSON Freestyle Diagnostic Ultrasound System,ACUSON S1000, S2000, S3000 Diagnostic Ultrasound Systems, ACUSON P200 Diagnostic Ultrasound System, ACUSON P500 Diagnostic Ultrasound System, ACUSON NX3, NX3 Elite

ApplicantSiemens Medical Solutions USA, Inc., Issaquah WA, US
DecisionSubstantially Equivalent, Oct 15, 2020
ReceivedSep 15, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K202683

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.