meddevicedb.com FDA Device Reference

DAYTON WATER SYSTEMS ULTRAPURE WATER TREATMENT SYSTEMS FOR HEMODIALYSIS

K021352 Class II Special
Decision Date
2002-08-01
Sponsor / Applicant
Dayton Water Systems

Technical Specification

510(k) Submission ID K021352
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2002-08-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DAYTON WATER SYSTEMS ULTRAPURE WATER TREATMENT SYSTEMS FOR HEMODIALYSIS received FDA 510(k) clearance under submission number K021352, sponsored by Dayton Water Systems. 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 2002-08-01.

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.