# K240975: Electrosurgical Generator (ES-100); Electrosurgical Generator (ES-300)

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Taktvoll Technology Co., Ltd.
- Decided: Dec 23, 2024 after 257 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: 5 generations back to K933002 (1994). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K134054: Bovie Ids-310 High Frequency Electrosurgical Generator, Aaron A3350 High Frequency Electrosurgical Generator, Bovie Medical Corporation (2014) Summary page 5.

## Indications for use
The Electrosurgical Generator is used to deliver RF energy via an assortment of surgical devices to cut and coagulate different kinds of tissue.

Source page: https://510kreport.com/device/K240975
Methodology: https://510kreport.com/methodology