meddevicedb.com FDA Device Reference

RenaPure Endotoxin Retentive Filter

K231410 Class II Traditional
Decision Date
2023-07-19
Sponsor / Applicant
Evoqua Water Technologies, LLC

Technical Specification

510(k) Submission ID K231410
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2023-07-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RenaPure Endotoxin Retentive Filter received FDA 510(k) clearance under submission number K231410, sponsored by Evoqua Water Technologies, 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 2023-07-19.

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.