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MENTOR SELF-CATH CLOSED SYSTEM

K003873 Class II Traditional
Decision Date
2001-03-29
Sponsor / Applicant
Mentor Corp.

Technical Specification

510(k) Submission ID K003873
Product Code FCM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2001-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MENTOR SELF-CATH CLOSED SYSTEM received FDA 510(k) clearance under submission number K003873, sponsored by Mentor Corp.. 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 2001-03-29.

Classification & Regulation

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