ClearanceBrief
510(k) K845030 ยท EAM Screen, Intensifying, Radiographic

CRONEX SR342-QUANTA FAST DETAIL-INTENSI-SCREENS

ApplicantE.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US
DecisionSubstantially Equivalent, Feb 26, 1985
ReceivedDec 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K845030

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.