meddevicedb.com FDA Device Reference

ANGEL OF WATER COLON HYDROTHERAPY SYSTEM

K003720 Class II Traditional
Decision Date
2002-06-27
Sponsor / Applicant
Lifestream Purfication Systems, LLC

Technical Specification

510(k) Submission ID K003720
Product Code KPL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5220
Decision Date 2002-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANGEL OF WATER COLON HYDROTHERAPY SYSTEM received FDA 510(k) clearance under submission number K003720, sponsored by Lifestream Purfication Systems, LLC. 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 2002-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code KPL and 21 CFR 876.5220, within the Gastroenterology, Urology review panel as a Class II device.