Cleared Traditional

AquaA

K252181 · Fresenius Medical Care North America · Gastroenterology & Urology
Sep 2025
Decision
60d
Days
Class 2
Risk

About This 510(k) Submission

K252181 is an FDA 510(k) clearance for the AquaA, a Subsystem, Water Purification (Class II — Special Controls, product code FIP), submitted by Fresenius Medical Care North America (Waltham, US). The FDA issued a Cleared decision on September 9, 2025, 60 days after receiving the submission on July 11, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5665.

Submission Details

510(k) Number K252181 FDA.gov
FDA Decision Cleared SESE
Date Received July 11, 2025
Decision Date September 09, 2025
Days to Decision 60 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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