# K960066: Immulite Acth

- Pathway: 510(k) (Traditional)
- Applicant: Diagnostic Products Corp.
- Decided: Feb 16, 1996 after 42 days
- Product code: CKG (Radioimmunoassay, Acth)
- Device class: 2
- Regulation: 21 CFR 862.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K060585: Roche Elecsys- Acth,Acth Calset,Acth Calcheck,Precicontrol Acth (2006), 4 descendants of its own
- K111335: ST Aia-Pack Acth, and ST Aia-Pack Acth Calibrator Set Model 025221 and 025321 (2011), 1 descendant of its own
- K223867: Ids Acth II (2023), 0 descendants of its own
- K143296: AIA-PACK C-Peptide Control Set (2014), 0 descendants of its own
- K131662: Immulite 2000 Acth Calibration Verification Material (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K960066
Methodology: https://510kreport.com/methodology