ClearanceBrief
510(k) K032280 ยท IZL System, X-Ray, Mobile

SIREMOBIL ISO-C 3D

ApplicantSiemens AG, Mavern PA, US
DecisionSubstantially Equivalent, Sep 10, 2003
ReceivedJul 24, 2003
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K032280

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.