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SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEM

K070939 Class II Special
Decision Date
2007-06-01
Sponsor / Applicant
Coloplast Manufacturing Us, LLC

Technical Specification

510(k) Submission ID K070939
Product Code FCM
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 2007-06-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEM received FDA 510(k) clearance under submission number K070939, sponsored by Coloplast Manufacturing Us, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2007-06-01.

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.