meddevicedb.com FDA Device Reference

ELECTRODE FOR URINARY INCONTINENCE

K140265 Class II Traditional
Decision Date
2015-01-23
Sponsor / Applicant
Guangzhou Finecure Medical Equipment Co.,Ltd

Technical Specification

510(k) Submission ID K140265
Product Code KPI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5320
Decision Date 2015-01-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRODE FOR URINARY INCONTINENCE received FDA 510(k) clearance under submission number K140265, sponsored by Guangzhou Finecure Medical Equipment Co.,Ltd. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2015-01-23.

Classification & Regulation

This clearance is catalogued under FDA product code KPI and 21 CFR 876.5320, within the Gastroenterology, Urology review panel as a Class II device.