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RUSCH SIMPLASTIC COUNCILL TIP CATHETER

K974419 Class II Traditional
Decision Date
1998-01-27
Sponsor / Applicant
Rusch, Inc.

Technical Specification

510(k) Submission ID K974419
Product Code EZL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5130
Decision Date 1998-01-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RUSCH SIMPLASTIC COUNCILL TIP CATHETER received FDA 510(k) clearance under submission number K974419, sponsored by Rusch, 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 1998-01-27.

Classification & Regulation

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