# K143024: CAS-One Liver

- Pathway: 510(k) (Traditional)
- Applicant: Cascination AG
- Decided: Apr 28, 2015 after 189 days
- Product code: OEW (Tracking, Soft Tissue, Intraoperative)
- Device class: 2
- Regulation: 21 CFR 882.4560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K882383 (1988). 18 ancestors in all.
No later device cites it as a predicate yet.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101979: Explorer Liver (Passive Tracking), Pathfinder Therapeutics, Inc. (2011) Summary page 5.

## Indications for use
The CAS-One Liver system is indicated for open liver surgical procedures where image guidance may be appropriate and where the patient can tolerate long apneic periods under general anesthesia

Source page: https://510kreport.com/device/K143024
Methodology: https://510kreport.com/methodology
