ClearanceBrief
510(k) K190476 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic

FUJIFILM Sonosite Vevo MD Imaging System

ApplicantFUJIFILM Sonosite, Inc., Bothell WA, US
DecisionSubstantially Equivalent, Mar 15, 2019
ReceivedFeb 27, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190476

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.