# K904302: Dupont Dimension (R) Ethyl Alcohol (Alc) Method

- Pathway: 510(k) (Traditional)
- Applicant: E.I. Dupont DE Nemours & Co., Inc.
- Decided: Oct 12, 1990 after 23 days
- Product code: DIC (Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method)
- Device class: 2
- Regulation: 21 CFR 862.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K071811: Etoh Flex Reagent Cartridge (DF22) (2007), 0 descendants of its own
- K070853: Dimension Vista Etoh Flex Reagent Cartridge, Model K5022 (2007), 0 descendants of its own
- K061792: Dimension Vista Ethyl Alcohol (Alc), Alkaline Phosphatase (Alp), Calcium (CA0 Flex, Lactic Acid (LA) Flex Reagent Cartri (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K904302
Methodology: https://510kreport.com/methodology