ClearanceBrief
510(k) K920031 ยท JAC System, X-Ray, Film Marking, Radiographic

KODAK X-OMATIC IDENT. CAMERA MAMMOGRAPHY UPGRADE

ApplicantEastman Kodak Company, Rochester NY, US
DecisionSubstantially Equivalent, Feb 12, 1992
ReceivedJan 3, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920031

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.