meddevicedb.com FDA Device Reference

Z-Robot Patient Positioning System

K182683 Class II Traditional
Decision Date
2019-06-27
Sponsor / Applicant
Chinan Biomedical Technology, Inc.

Technical Specification

510(k) Submission ID K182683
Product Code JAI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5770
Decision Date 2019-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Z-Robot Patient Positioning System received FDA 510(k) clearance under submission number K182683, sponsored by Chinan Biomedical Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2019-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code JAI and 21 CFR 892.5770, within the Radiology review panel as a Class II device.