# K152059: Disposable General Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Modern Medical Equipment Manufacturing Limited
- Decided: Apr 21, 2016 after 272 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 K853291 (1985). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091672: Disposable Grounding Pad Series and Electrode Series, Shuyou Electric Medical Science Co., Ltd. (2009) Summary page 5.

## Most influential descendants
- K171707: GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, GA-F1A (2017), 0 descendants of its own

## Indications for use
The electrode is used to cut and / or coagulate soft tissues by means of high frequency electrical current during an electrosurgical procedure.

Source page: https://510kreport.com/device/K152059
Methodology: https://510kreport.com/methodology