meddevicedb.com FDA Device Reference

Liver fat ultrasound quantitative system, The FattaLab (FL-CC M1, FL-CC M1_Pro)

K253221 Class II Traditional
Decision Date
2026-02-06
Sponsor / Applicant
Eieling Technology (Shenzhen) Limited

Technical Specification

510(k) Submission ID K253221
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2026-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Liver fat ultrasound quantitative system, The FattaLab (FL-CC M1, FL-CC M1_Pro) received FDA 510(k) clearance under submission number K253221, sponsored by Eieling Technology (Shenzhen) Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.