# The DU Pont Co.

- Location (FDA's records): Wilmington, DE
- FDA decisions: 13 (1988–1995): 13 510(k) clearances
- Product codes: LMC (2), KLI (2), KHQ (1), JIT (1), IXA (1), LEH (1), DLJ (1), KLS (1), KDL (1), JIS (1), CEL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Sangstat Medical Corp.: 1 (https://510kreport.com/company/sangstat-medical)

## Its most-cited devices
- K900492: Labeling Change - Viaspan (TM) (Belzer UW) (1990), cited by 1

## Recent decisions
- K953475: CDS Compact Daylight Cassette for Video Imaging (Oct 7, 1995)
- K953477: Modular Daylight Cassette for Video Imaging (Oct 7, 1995)
- K952891: Cronex Low Absorption Cassette (Jul 13, 1995)
- K945125: Dupont Aca Vancomycin (Vanc) Method (Mar 10, 1995)
- K943704: Lipase Calibrator (Sep 14, 1994)
- K900492: Labeling Change - Viaspan (TM) (Belzer UW) (Mar 20, 1990)
- K885259: Aca Thyronine Uptake (TU E) Method (Feb 17, 1989)
- K885258: Aca Thyroxine (T4 E) Method (Feb 17, 1989)

Source page: https://510kreport.com/company/du-pont