meddevicedb.com FDA Device Reference

WIDE 3MP GRAYSCALE TFT LCD MONITOR IF2103A

K032174 Class II Traditional
Decision Date
2003-07-24
Sponsor / Applicant
Wide Corporation

Technical Specification

510(k) Submission ID K032174
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2003-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WIDE 3MP GRAYSCALE TFT LCD MONITOR IF2103A received FDA 510(k) clearance under submission number K032174, sponsored by Wide Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-07-24.

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.