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RENACLEAR DIALYZER CLEANING SYSTEM

K991851 Class II Traditional
Decision Date
1999-08-30
Sponsor / Applicant
Minntech Corp.

Technical Specification

510(k) Submission ID K991851
Product Code LIF
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1999-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RENACLEAR DIALYZER CLEANING SYSTEM received FDA 510(k) clearance under submission number K991851, sponsored by Minntech 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 1999-08-30.

Classification & Regulation

This clearance is catalogued under FDA product code LIF and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.