ClearanceBrief
510(k) K160790 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

Acclarix LX8 Diagnostic Ultrasound System

ApplicantEdan Instruments, Inc., Shenzhen, CN
DecisionSubstantially Equivalent, Apr 4, 2016
ReceivedMar 22, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160790

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.