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WIJAY EZ-VOID EXTERNAL CATHETER VALVE

K140562 Class II Traditional
Decision Date
2014-06-16
Sponsor / Applicant
Leomed, LLC

Technical Specification

510(k) Submission ID K140562
Product Code KNY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2014-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WIJAY EZ-VOID EXTERNAL CATHETER VALVE received FDA 510(k) clearance under submission number K140562, sponsored by Leomed, LLC. 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 2014-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code KNY and 21 CFR 876.5130, within the Gastroenterology, Urology review panel as a Class II device.