Cleared Abbreviated

K103724 - 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030)

K103724 is an FDA 510(k) clearance for 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX ..., manufactured by Eizo GmbH. The device is a Class 2 Radiology device with product code LLZ cleared through the Abbreviated 510(k) pathway after a 169-day FDA review.

K103724 · Eizo GmbH · Radiology device
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Jun 2011
Decision
169d
Days
Class 2
Risk

K103724 is an FDA 510(k) clearance for the 10 MP GRAYSCALE FLAT PANEL DISPLAY (GX 1030). Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by Eizo GmbH (Karlsruhe, DE). The FDA issued a Cleared decision on June 8, 2011 after a review of 169 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - the FDA radiology and imaging software oversight framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Incremental AI imaging tool. Standards-verified equivalence. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all Eizo GmbH devices

FDA 510(k) Submission Details - K103724

510(k) Number K103724 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 21, 2010
Decision Date June 08, 2011
Days to Decision 169 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
62d slower than avg
Panel avg: 107d · This submission: 169d
Pathway characteristics
Standards-based clearance path.

LLZ Device Classification - Class 2, Special Controls

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Radiology devices follow this clearance model.

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