meddevicedb.com FDA Device Reference

BCM2-Body Composition Monitor

K250634 Class II Traditional
Decision Date
2025-11-24
Sponsor / Applicant
Fresenius Medical Care Renal Therapies Group, LLC

Technical Specification

510(k) Submission ID K250634
Product Code DSB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2770
Decision Date 2025-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BCM2-Body Composition Monitor received FDA 510(k) clearance under submission number K250634, sponsored by Fresenius Medical Care Renal Therapies Group, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code DSB and 21 CFR 870.2770, within the Cardiovascular review panel as a Class II device.