# K935806: Immulite Dhea-S04

- Pathway: 510(k) (Traditional)
- Applicant: Diagnostic Products Corp.
- Decided: Apr 26, 1994 after 145 days
- Product code: JKC (Radioimmunoassay, Dehydroepiandrosterone (Free And Sulfate))
- Device class: 1
- Regulation: 21 CFR 862.1245
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K040181: Access Dhea-S Reagent Assay (2004), 1 descendant of its own
- K111762: ST Aia-Pack Dhea-S Calibrator Set (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K935806
Methodology: https://510kreport.com/methodology