meddevicedb.com FDA Device Reference

uWS-CT

K183170 Class II Traditional
Decision Date
2019-06-24
Sponsor / Applicant
Shanghai United Imaging Healthcare Co., Ltd.

Technical Specification

510(k) Submission ID K183170
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2019-06-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

uWS-CT received FDA 510(k) clearance under submission number K183170, 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 2019-06-24.

Classification & Regulation

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