# K140265: Electrode for Urinary Incontinence

- Pathway: 510(k) (Traditional)
- Applicant: Guangzhou Finecure Medical Equipment Co.,Ltd
- Decided: Jan 23, 2015 after 354 days
- Product code: KPI (Stimulator, Electrical, Non-Implantable, For Incontinence)
- Device class: 2
- Regulation: 21 CFR 876.5320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K891773 (1989). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122194: Life-Care Vaginal Probe Life-Care Anal Probe, Everyway Medical Instruments Co.,Ltd (2013) Summary page 6.

## Indications for use
The Urinary Incontinence Probe, model PR-51 Vaginal Probe & PR-52 Anal Probe are intended to provide electromyographic feedback from pelvic musculature or electrical stimulation to pelvic musculature for the purpose of rehabilitation of weak pelvic floor muscles and restoration of neuromuscular control during the treatment of urinary incontinence.

Source page: https://510kreport.com/device/K140265
Methodology: https://510kreport.com/methodology