# K232763: Electrode Handpieces (VCT, RFTV, BMDT series)

- Pathway: 510(k) (Special)
- Applicant: RF Medical Co., Ltd.
- Decided: Oct 4, 2023 after 26 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: 2 generations back to K180999 (2018). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K193355: Electrodes Handpieces for Mygen V-1000 RF System, RF Medical Co., Ltd. (2020) Summary page 4.

## Indications for use
Electrodes Handpieces (VCT, RFTV, BMDT) are indicated for coagulation and ablation of tissue when used in conjunction with Mygen V-1000 RF generator (K193355) and M-3004 RF generator (K221277).

Source page: https://510kreport.com/device/K232763
Methodology: https://510kreport.com/methodology