# K232240: Microwave Ablation System (BD-GT)

- Pathway: 510(k) (Traditional)
- Applicant: Betters (Suzhou) Medical Co., Ltd.
- Decided: Nov 13, 2023 after 108 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.
1 later device descends from it; 1 cites it directly.
0 of 46 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.

## Most influential descendants
- K252632: Microwave Ablation Device (2026), 0 descendants of its own

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

Source page: https://510kreport.com/device/K232240
Methodology: https://510kreport.com/methodology