ClearanceBrief
510(k) K910354 ยท JAC System, X-Ray, Film Marking, Radiographic

DU PONT IDENTIFICATION CAMERA

ApplicantDupont Medical Products, Wilmington DE, US
DecisionSubstantially Equivalent, Mar 29, 1991
ReceivedJan 29, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910354

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.