Cleared Traditional

K243384 - Belzer UW® Cold Storage Solution (BTLBUW-001) (FDA 510(k) Clearance)

Mar 2025
Decision
151d
Days
Class 2
Risk

K243384 is an FDA 510(k) clearance for the Belzer UW® Cold Storage Solution (BTLBUW-001). This device is classified as a System, Perfusion, Kidney (Class II - Special Controls, product code KDN).

Submitted by Bridge TO Life (Northbrook, US). The FDA issued a Cleared decision on March 31, 2025, 151 days after receiving the submission on October 31, 2024.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5880.

Submission Details

510(k) Number K243384 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 31, 2024
Decision Date March 31, 2025
Days to Decision 151 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code KDN - System, Perfusion, Kidney
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5880