Cleared Traditional

K133708 - MD302C4 29.8 DIAGNOSTIC IMAGING LCD MONITOR

K133708 is an FDA 510(k) clearance for MD302C4 29.8 DIAGNOSTIC IMAGING LCD MONITOR, manufactured by Nec Display Solutions , Ltd.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K133708 · Nec Display Solutions , Ltd. · Radiology device
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Feb 2014
Decision
72d
Days
Class 2
Risk

K133708 is an FDA 510(k) clearance for the MD302C4 29.8 DIAGNOSTIC IMAGING LCD MONITOR. 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 Nec Display Solutions , Ltd. (New Taipei City, TW). The FDA issued a Cleared decision on February 14, 2014 after a review of 72 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Incremental AI imaging tool. Moderate equivalence dependency. 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 Nec Display Solutions , Ltd. devices

FDA 510(k) Submission Details - K133708

510(k) Number K133708 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 04, 2013
Decision Date February 14, 2014
Days to Decision 72 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
35d faster than avg
Panel avg: 107d · This submission: 72d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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.

Regulatory Peers - LLZ System, Image Processing, Radiological

All 1236
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K133708.
SCENIUM
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K133730 · Konica Minolta, Inc. · Jan 2014
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