meddevicedb.com FDA Device Reference

uWS-MR

K192601 Class II Traditional
Decision Date
2020-06-01
Sponsor / Applicant
Shanghai United Imaging Healthcare Co., Ltd.

Technical Specification

510(k) Submission ID K192601
Product Code QIH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2020-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

uWS-MR received FDA 510(k) clearance under submission number K192601, 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 2020-06-01.

Classification & Regulation

This clearance is catalogued under FDA product code QIH and 21 CFR 892.2050, within the Radiology review panel as a Class II device.