ClearanceBrief
510(k) K893510 ยท EAM Screen, Intensifying, Radiographic

CRONEX QUANTA V RARE EARTH INTENSIFYING SCREEN

ApplicantE.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US
DecisionSubstantially Equivalent, Jun 23, 1989
ReceivedMay 5, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893510

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.