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ULTRAPURE WATER TREATMENT SYSTEM FOR HEMODIALYSIS

K981680 Class II Traditional
Decision Date
1998-12-31
Sponsor / Applicant
Dayton Water Systems

Technical Specification

510(k) Submission ID K981680
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 1998-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRAPURE WATER TREATMENT SYSTEM FOR HEMODIALYSIS received FDA 510(k) clearance under submission number K981680, sponsored by Dayton Water Systems. 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 1998-12-31.

Classification & Regulation

This clearance is catalogued under FDA product code FIP and 21 CFR 876.5665, within the Gastroenterology, Urology review panel as a Class II device.