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LMD-2451MT LCD Monitor

by Sony Electronics, Inc.

510(k) K113203

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK113203 Date24 Feb 2012ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

Full name
Sony Lmd-2451MT LCD Monitor
510(k) Number
FDA Product Code
GCJ
Device Class
Class II
Regulation
21 CFR Part 876.1500
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 1 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The LMD-2451MT LCD Monitor is a medical grade display device designed for real-time visualization of 2D and 3D color video images. It is intended for use with surgical endoscopic/laparoscopic camera systems and other compatible medical imaging systems, providing high-definition widescreen output. The monitor incorporates professional-grade technology, including 3D display capabilities and optimized image quality features such as ChromaTRU technology. Its primary function is to enhance surgical visualization during minimally invasive procedures.

This monitor is supplied as a reusable, non-sterile device intended for use in hospital operating rooms and clinical settings. It features a 24-inch LCD panel with polarized 3D viewing support, enabling surgeons to wear lightweight glasses while maintaining clear image fidelity. The device includes user memory functions and chroma phase control for adjustable image optimization. Authorized for commercial distribution in the United States under FDA 510(k) clearance (K113203), it adheres to medical imaging standards for surgical applications.

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Questions

AI-generated answers, 1 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the primary use of the Sony LMD-2451MT LCD Monitor?

    The LMD-2451MT is designed specifically for real-time visualization of 2D and 3D color video images during surgical procedures. It is intended for use with endoscopic/laparoscopic camera systems and other compatible medical imaging devices, providing high-definition widescreen output to improve surgical precision in minimally invasive operations.

  • Is the LMD-2451MT a single-use or reusable device?

    The LMD-2451MT is a reusable, non-sterile device. It is engineered for repeated use in hospital operating rooms and clinical settings, ensuring durability and reliability for continuous surgical applications.

  • What display features does the monitor include for 3D visualization?

    The monitor features a 24-inch LCD panel with polarized 3D viewing support, allowing surgeons to wear lightweight glasses while maintaining high image fidelity. Additional features include user memory functions and chroma phase control for adjustable image optimization, ensuring clarity and adaptability during procedures.

  • How is the monitor supplied, and what are its key specifications?

    The monitor is supplied as a standalone unit, ready for integration with compatible medical imaging systems. It includes a 24-inch display with professional-grade technology, such as ChromaTRU for enhanced color accuracy and optimized image quality. The device adheres to medical imaging standards for surgical applications and is authorized for commercial distribution in the U.S. under FDA 510(k) clearance.

  • What regulatory pathway was followed for this device’s clearance?

    The LMD-2451MT underwent a traditional 510(k) review process through the FDA, with a decision of substantial equivalence (SESE) made by the Gastroenterology and Urology advisory committees. The clearance number is K113203, and the device is classified under product code GCJ.