ClearanceBrief
510(k) K082119 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

APLIO XG DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SSA - 790A VERSION 3.0

ApplicantToshiba America Medical Systems, In.C, Tustin CA, US
DecisionSubstantially Equivalent, Aug 12, 2008
ReceivedJul 28, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082119

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.