meddevicedb.com FDA Device Reference

uMR 680

K243397 Class II Traditional
Decision Date
2025-07-16
Sponsor / Applicant
Shanghai United Imaging Healthcare Co., Ltd.

Technical Specification

510(k) Submission ID K243397
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2025-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

uMR 680 received FDA 510(k) clearance under submission number K243397, sponsored by Shanghai United Imaging Healthcare Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.