ClearanceBrief
510(k) K894806 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic

SIEMENS ENDO-P-PROBE

ApplicantSiemens Medical Solutions USA, Inc., Pleasanton CA, US
DecisionSubstantially Equivalent, Oct 5, 1989
ReceivedJul 28, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894806

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.