Cleared Special

K073340 - COLOR LCD MONITOR

K073340 is the FDA 510(k) clearance for COLOR LCD MONITOR by Eizo Nanao Corporation. It is a Class 2 Radiology device (product code LLZ) cleared through the Special 510(k) pathway after a 21-day FDA review.

K073340 · Eizo Nanao Corporation · Radiology device
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Dec 2007
Decision
21d
Days
Class 2
Risk

K073340 is an FDA 510(k) clearance for the COLOR LCD MONITOR, FLEXSCAN MX300W. 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 Nanao Corporation (Hakusan, Ishikawa-Ken, JP). The FDA issued a Cleared decision on December 19, 2007 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Incremental AI imaging tool. Low regulatory complexity profile. 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 Nanao Corporation devices

Submission Details

510(k) Number K073340 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 28, 2007
Decision Date December 19, 2007
Days to Decision 21 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
86d faster than avg
Panel avg: 107d · This submission: 21d
Pathway characteristics
Modification to existing cleared device.

Device Classification

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.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 1127
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K073340.
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XIDF-100A/B1 IMAGE PROCESSOR
K073259 · Toshiba America Medical Systems, In.C · Dec 2007
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K072986 · Ge Healthcare · Nov 2007
GE ECHOPAC
K072952 · General Electric Co. · Nov 2007
20.8-INCH (53CM) COLOR LCD MONITOR CDL2119A (CCL352I2)
K072065 · Totoku Electric Co., Ltd. · Aug 2007