Cleared Traditional

K250471 - AquaC UNO H (FDA 510(k) Clearance)

Nov 2025
Decision
269d
Days
Class 2
Risk

K250471 is an FDA 510(k) clearance for the AquaC UNO H. This device is classified as a Subsystem, Water Purification (Class II - Special Controls, product code FIP).

Submitted by Fresenius Medical Care Renal Therapies Group, LLC (Waltham, US). The FDA issued a Cleared decision on November 14, 2025, 269 days after receiving the submission on February 18, 2025.

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

Submission Details

510(k) Number K250471 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 18, 2025
Decision Date November 14, 2025
Days to Decision 269 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