# Dupont Medical Products

- Location (FDA's records): Wilmington, DE
- FDA decisions: 28 (1991–1995): 28 510(k) clearances
- Product codes: IXA (2), JKA (2), JIS (2), JHS (2), EAM (1), CEP (1), CEM (1), JIQ (1), JAC (1), KXT (1), CGJ (1), CFT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dade Behring, Inc.: 5 (https://510kreport.com/company/dade-behring)

## Its most-cited devices
- K943024: Kinase Isoenzyme (1994), cited by 1
- K944932: Phenobarbital Flex Reagent Cartridge (1994), cited by 1
- K936201: Urinary Albumin Calibrator (1994), cited by 1
- K942640: Dupont Dimension Amylase Method (1994), cited by 1
- K941584: Creatine Kinase Method (1994), cited by 1

## Recent decisions
- K952815: Dupont Lipase Calibrator (Aug 31, 1995)
- K950920: Dupont Dimension Total Protein Method (Aug 11, 1995)
- K952816: Lipase Flex Reagent Cartridge (Jul 20, 1995)
- K952412: Dupont Aca (R) Urine Druge OS Abuse Control (Jun 23, 1995)
- K945280: Dupont Dimension C-Reactive Protein Method (Mar 9, 1995)
- K944932: Phenobarbital Flex Reagent Cartridge (Dec 28, 1994)
- K941050: Dupont Aca Star (Nov 10, 1994)
- K943996: Dupont Aca Plus Luteinizing Hormone (LH) Method (Oct 20, 1994)

Source page: https://510kreport.com/company/dupont-medical-products