# K201262: Microwave Therapeutic System

- Pathway: 510(k) (Traditional)
- Applicant: Nanjing Eco Microwave System Co., Ltd.
- Decided: Jul 9, 2021 after 424 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: 11 generations back to K870028 (1987). 43 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 48 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183153: Microwave Ablation System, Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. (2019) Summary page 4.

## Most influential descendants
- K232240: Microwave Ablation System (BD-GT) (2023), 1 descendant of its own
- K252632: Microwave Ablation Device (2026), 0 descendants of its own
- K241827: Microwave Ablation Generator (KY-2000A, KY-2100A) (2024), 0 descendants of its own
- K233140: Microwave Ablation Device (Exceed S10U); Sterile Microwave Ablation Probe (Exact) (2024), 0 descendants of its own

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

Source page: https://510kreport.com/device/K201262
Methodology: https://510kreport.com/methodology