# K171707: GA-B, GA-C, GA-E, GA-I, GA-S, GA-W3A, GA-F3A, GA-IL, GA-SL, GA-W3B, GA-F1A

- Pathway: 510(k) (Traditional)
- Applicant: Gowoonsesang Cosmetics Co., Ltd.
- Decided: Aug 8, 2017 after 61 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: 6 generations back to K853291 (1985). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K152059: Disposable General Electrode, Modern Medical Equipment Manufacturing Limited (2016) Summary page 4.

## Indications for use
The Single Use RF electrode (Needle Type) is a monopolar electrosurgical electrode indicated for coagulation of soft tissue when it used in conjunction with compatible radio frequency electrosurgical device.

Source page: https://510kreport.com/device/K171707
Methodology: https://510kreport.com/methodology