ClearanceBrief
510(k) K931930 ยท IZO Generator, High-Voltage, X-Ray, Diagnostic

POYDOROS LX

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Sep 7, 1993
ReceivedApr 16, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931930

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.