Cleared Traditional

K231410 - RenaPure Endotoxin Retentive Filter (FDA 510(k) Clearance)

Jul 2023
Decision
65d
Days
Class 2
Risk

K231410 is an FDA 510(k) clearance for the RenaPure Endotoxin Retentive Filter. This device is classified as a Subsystem, Water Purification (Class II - Special Controls, product code FIP).

Submitted by Evoqua Water Technologies, LLC (Tewksbury, US). The FDA issued a Cleared decision on July 19, 2023, 65 days after receiving the submission on May 15, 2023.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5665.

Submission Details

510(k) Number K231410 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 15, 2023
Decision Date July 19, 2023
Days to Decision 65 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FIP - Subsystem, Water Purification
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5665

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