meddevicedb.com FDA Device Reference

HEMO-RO WATER PURIFICATION SYS

K841403 Class II Traditional
Decision Date
1984-07-06
Sponsor / Applicant
Millipore Corp.

Technical Specification

510(k) Submission ID K841403
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 1984-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMO-RO WATER PURIFICATION SYS received FDA 510(k) clearance under submission number K841403, sponsored by Millipore 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 1984-07-06.

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.