# K222429: Ellusa Reusable Bipolar Cable

- Pathway: 510(k) (Special)
- Applicant: Ellusa, LLC
- Decided: Sep 9, 2022 after 29 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- 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: 7 generations back to K954171 (1996). 12 ancestors in all.
No later device cites it as a predicate yet.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K202558: Ellusa Bipolar Wands, Ellusa, LLC (2020) Summary page 4.

## Indications for use
The Ellusa Reusable Bipolar Cable is intended to transfer power from an RF Generator to Bipolar Electrodes.

Source page: https://510kreport.com/device/K222429
Methodology: https://510kreport.com/methodology