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FIBERFLO HOLLOW FIBER CAPSULE WATER FILTERS

K983126 Class II Traditional
Decision Date
1999-03-08
Sponsor / Applicant
Minntech Corp.

Technical Specification

510(k) Submission ID K983126
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 1999-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIBERFLO HOLLOW FIBER CAPSULE WATER FILTERS received FDA 510(k) clearance under submission number K983126, sponsored by Minntech 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 1999-03-08.

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.