ClearanceBrief
510(k) K834484 ยท EAM Screen, Intensifying, Radiographic

CRONEX SR-337

ApplicantE.I. Dupont DE Nemours & Co., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 21, 1984
ReceivedDec 1, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834484

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.