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MENTOR UROLOGY TRIPLE RIB OCCLUSION WRAP FOR MALE INCONTINENCE

K970308 Class I Traditional
Decision Date
1997-04-02
Sponsor / Applicant
Mentor Urology, Inc.

Technical Specification

510(k) Submission ID K970308
Product Code FHA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5160
Decision Date 1997-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MENTOR UROLOGY TRIPLE RIB OCCLUSION WRAP FOR MALE INCONTINENCE received FDA 510(k) clearance under submission number K970308, sponsored by Mentor Urology, Inc.. 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 1997-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code FHA and 21 CFR 876.5160, within the Gastroenterology, Urology review panel as a Class I device.