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AIW WATER SYSTEM FOR HEMODIALYSIS

K001282 Class II Traditional
Decision Date
2000-12-15
Sponsor / Applicant
American Industrial Water

Technical Specification

510(k) Submission ID K001282
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2000-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AIW WATER SYSTEM FOR HEMODIALYSIS received FDA 510(k) clearance under submission number K001282, sponsored by American Industrial Water. 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 2000-12-15.

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.