# K082279: Epicor Ablation Control System, Model Acs-US-2, Acs-Eur-2

- Pathway: 510(k) (Special)
- Applicant: St Jude Medical
- Decided: Sep 16, 2008 after 36 days
- Product code: OCL (Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K942299 (1995). 51 ancestors in all.
No later device cites it as a predicate yet.
0 of 52 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080292: Epicor Ablation System, St Jude Medical (2008) Summary page 1.

## Indications for use
The Epicor Ablation System is intended for the ablation of cardiac tissue during cardiac surgery.

Source page: https://510kreport.com/device/K082279
Methodology: https://510kreport.com/methodology