ClearanceBrief
510(k) K852502 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

AMENDMENT ULTRASOUND SCANNER TYPE 1842/1846/1849

ApplicantBruel & Kjaer Industri A/S, Denmark, DK
DecisionSubstantially Equivalent, Oct 23, 1986
ReceivedJun 12, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852502

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.