meddevicedb.com FDA Device Reference

uMR 680

K240744 Class II Special
Decision Date
2024-04-10
Sponsor / Applicant
Shanghai United Imaging Healthcare Co., Ltd.

Technical Specification

510(k) Submission ID K240744
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2024-04-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

uMR 680 received FDA 510(k) clearance under submission number K240744, sponsored by Shanghai United Imaging Healthcare Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-04-10.

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.