Cleared Traditional

K151883 - 5MP Monochrome LCD Monitor, RadiForce GX540

K151883 is an FDA 510(k) clearance for 5MP Monochrome LCD Monitor, manufactured by Eizo Corporation. The device is a Class 2 Radiology device with product code PGY cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K151883 · Eizo Corporation · Radiology device
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Jul 2015
Decision
21d
Days
Class 2
Risk

K151883 is an FDA 510(k) clearance for the 5MP Monochrome LCD Monitor, RadiForce GX540. Classified as Display, Diagnostic Radiology (product code PGY), Class II - Special Controls.

Submitted by Eizo Corporation (Hakusan, JP). The FDA issued a Cleared decision on July 30, 2015 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Eizo Corporation devices

FDA 510(k) Submission Details - K151883

510(k) Number K151883 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 09, 2015
Decision Date July 30, 2015
Days to Decision 21 days
Submission Type Traditional
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
Predicate-based equivalence. No clinical trials required.

PGY Device Classification - Class 2, Special Controls

Product Code PGY Display, Diagnostic Radiology
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
Definition The Device Is Intended For Use In Displaying Radiological Images For Review, Analysis, And Diagnosis By Trained Medical Practitioners.
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 - PGY Display, Diagnostic Radiology

All 134
Devices cleared under the same product code (PGY) and FDA review panel - the closest regulatory comparables to K151883.
Hisense 2MP/3MP LCD Monitor (HMD2C21/HMD3C21)
K152030 · Qingdao Hisense Medical Equipment Co., Ltd. · Sep 2015
JUSHA-C23C LCD Monitor
K151861 · Nanjing Jusha Display Technology Co., Ltd. · Sep 2015
JUSHA-C43 LCD Monitor
K151972 · Nanjing Jusha Display Technology Co., Ltd. · Sep 2015
Coronis Uniti
K151505 · Barco N.V. · Jul 2015
JUSHA-M23C LCD Monitor
K151238 · Nanjing Jusha Display Technology Co., Ltd. · Jun 2015
21.3 inch (54cm) Color LCD Monitor CCL210 (CL21210)
K151134 · Jvckenwood Corporation · May 2015