meddevicedb.com FDA Device Reference

BTI FILTRATION DEIONIZATION EXCHANGE TANK; BTI FILTRATION CARBON EXCHANGE TANK

K080703 Class II Traditional
Decision Date
2008-06-02
Sponsor / Applicant
4m Ventures, Inc.

Technical Specification

510(k) Submission ID K080703
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2008-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BTI FILTRATION DEIONIZATION EXCHANGE TANK; BTI FILTRATION CARBON EXCHANGE TANK received FDA 510(k) clearance under submission number K080703, sponsored by 4m Ventures, 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 2008-06-02.

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.