# K241827: Microwave Ablation Generator (KY-2000A, KY-2100A)

- Pathway: 510(k) (Traditional)
- Applicant: Canyon Medical, Inc.
- Decided: Sep 26, 2024 after 94 days
- Product code: NEY (System, Ablation, Microwave And 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: 12 generations back to K870028 (1987). 44 ancestors in all.
No later device cites it as a predicate yet.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201262: Microwave Therapeutic System, Nanjing Eco Microwave System Co., Ltd. (2021) Summary page 5.

## Indications for use
Microwave Ablation Generator is indicated for the coagulation (ablation) of soft tissue. The device is not intended for cardiac use.

Source page: https://510kreport.com/device/K241827
Methodology: https://510kreport.com/methodology