meddevicedb.com FDA Device Reference

NIO COLOR 3MP LED

K131295 Class II Special
Decision Date
2013-05-29
Sponsor / Applicant
Barco N.V.

Technical Specification

510(k) Submission ID K131295
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2013-05-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NIO COLOR 3MP LED received FDA 510(k) clearance under submission number K131295, sponsored by Barco N.V.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2013-05-29.

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.