Cleared Traditional

BCM2-Body Composition Monitor

K250634 · Fresenius Medical Care Renal Therapies Group, LLC · Gastroenterology & Urology
Nov 2025
Decision
266d
Days
Class 2
Risk

About This 510(k) Submission

K250634 is an FDA 510(k) clearance for the BCM2-Body Composition Monitor, a Plethysmograph, Impedance (Class II — Special Controls, product code DSB), submitted by Fresenius Medical Care Renal Therapies Group, LLC (Waltham, US). The FDA issued a Cleared decision on November 24, 2025, 266 days after receiving the submission on March 3, 2025. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 870.2770.

Submission Details

510(k) Number K250634 FDA.gov
FDA Decision Cleared SESE
Date Received March 03, 2025
Decision Date November 24, 2025
Days to Decision 266 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code DSB — Plethysmograph, Impedance
Device Class Class II — Special Controls
CFR Regulation 21 CFR 870.2770