FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 2 companies' records, each linked to the record.
As of Nov 15, 2026, FDA's public records list DuPont and its 2 subsidiaries with 281 510(k) clearances. The most recent is a 510(k) clearance dated Jul 24, 1996: ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY.
| Jul 24, 1996 | ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAYK951851 · LJO | 510(k) clearances |
| Sep 6, 1995 | CRONEX RADIATION THERAPY CASSETTEK953724 · IXA | 510(k) clearances |
| Sep 6, 1995 | CRONEX RADIATION THERAPY VERIFICATION CASSETTEK953725 · IXA | 510(k) clearances |
| Aug 31, 1995 | DUPONT LIPASE CALIBRATORK952815 · JIT | 510(k) clearances |
| Aug 11, 1995 | DUPONT DIMENSION TOTAL PROTEIN METHODK950920 · CEK | 510(k) clearances |
| Jul 20, 1995 | LIPASE FLEX REAGENT CARTRIDGEK952816 · CHI | 510(k) clearances |
| Jun 23, 1995 | DUPONT ACA(R) URINE DRUGE OS ABUSE CONTROLK952412 · DIF | 510(k) clearances |
| Jun 1, 1995 | DUPONT ACA DIGOXIN (DGN A) METHODK951441 · KXT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
