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AQUA CLEANSE

K150381 Class II Traditional
Decision Date
2015-09-11
Sponsor / Applicant
Quality Medical Supply, Inc.

Technical Specification

510(k) Submission ID K150381
Product Code KPL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5220
Decision Date 2015-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AQUA CLEANSE received FDA 510(k) clearance under submission number K150381, sponsored by Quality Medical Supply, Inc.. 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 2015-09-11.

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.