meddevicedb.com FDA Device Reference

LCD Monitor (MDEC-2523)

K243307 Class II Traditional
Decision Date
2024-12-13
Sponsor / Applicant
Barco N.V.

Technical Specification

510(k) Submission ID K243307
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2024-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LCD Monitor (MDEC-2523) received FDA 510(k) clearance under submission number K243307, sponsored by Barco N.V.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2024-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.