ClearanceBrief
510(k) K922208 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

FUKUDA DENSHI MODEL UF-4500

ApplicantFukuda Denshi USA, Inc., Redmond WA, US
DecisionSubstantially Equivalent, Aug 30, 1993
ReceivedMay 12, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922208

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.