ClearanceBrief
510(k) K041922 ยท IZL System, X-Ray, Mobile

GE TETHERED PORTABLE DIGITAL RADIOGRAPHIC DETECTOR

ApplicantGeneral Electric Co., Milwaukee WI, US
DecisionSubstantially Equivalent, Jul 28, 2004
ReceivedJul 16, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K041922

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.