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MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER

K012562 Class II Traditional
Decision Date
2002-02-08
Sponsor / Applicant
Medical Components, Inc.

Technical Specification

510(k) Submission ID K012562
Product Code MSD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5540
Decision Date 2002-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDCOMP 14.5F DOUBLE LUMEN HEMODIALYSIS CATHETER received FDA 510(k) clearance under submission number K012562, sponsored by Medical Components, 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 2002-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code MSD and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.