meddevicedb.com FDA Device Reference

NIO 5MP DISPLAY, MODEL E5620

K072875 Class II Traditional
Decision Date
2008-01-22
Sponsor / Applicant
Barcoview, Medical Imaging Systems

Technical Specification

510(k) Submission ID K072875
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2008-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIO 5MP DISPLAY, MODEL E5620 received FDA 510(k) clearance under submission number K072875, sponsored by Barcoview, Medical Imaging Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-01-22.

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.