ClearanceBrief
510(k) K902582 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

ALLERGAN HUMPHREY A/B SCAN , MODEL 835

ApplicantAllergan Humphrey, San Leandro CA, US
DecisionSubstantially Equivalent, Aug 14, 1990
ReceivedJun 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902582

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.