FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list The DU Pont Co. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Oct 7, 1995: MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGING.
| Oct 7, 1995 | MODULAR DAYLIGHT CASSETTE FOR VIDEO IMAGINGK953477 · LMC | 510(k) clearances |
| Oct 7, 1995 | CDS COMPACT DAYLIGHT CASSETTE FOR VIDEO IMAGINGK953475 · LMC | 510(k) clearances |
| Jul 13, 1995 | CRONEX LOW ABSORPTION CASSETTEK952891 · IXA | 510(k) clearances |
| Mar 10, 1995 | DUPONT ACA VANCOMYCIN (VANC) METHODK945125 · LEH | 510(k) clearances |
| Sep 14, 1994 | LIPASE CALIBRATORK943704 · JIT | 510(k) clearances |
| Mar 20, 1990 | LABELING CHANGE - VIASPAN(TM) (BELZER UW)K900492 · KDL | 510(k) clearances |
| Feb 17, 1989 | ACA THYRONINE UPTAKE (TU E) METHODK885259 · KHQ | 510(k) clearances |
| Feb 17, 1989 | ACA THYROXINE (T4 E) METHODK885258 · KLI | 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
