Cleared Traditional

K141743 - FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT

K141743 is an FDA 510(k) clearance for FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT, manufactured by Radiology Solutions, LLC. The device is a Class 2 Radiology device with product code MQB cleared through the Traditional 510(k) pathway after a 95-day FDA review.

K141743 · Radiology Solutions, LLC · Radiology device
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Oct 2014
Decision
95d
Days
Class 2
Risk

K141743 is an FDA 510(k) clearance for the FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Radiology Solutions, LLC (Naples, US). The FDA issued a Cleared decision on October 3, 2014 after a review of 95 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Radiology Solutions, LLC devices

FDA 510(k) Submission Details - K141743

510(k) Number K141743 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 30, 2014
Decision Date October 03, 2014
Days to Decision 95 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
12d faster than avg
Panel avg: 107d · This submission: 95d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MQB Device Classification - Class 2, Special Controls

Product Code MQB Solid State X-ray Imager (flat Panel/digital Imager)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
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 - MQB Solid State X-ray Imager (flat Panel/digital Imager)

All 289
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K141743.
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K142475 · DRTECH Corporation · Jan 2015
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K142003 · Fujifilm Medical System U.S.A., Inc. · Oct 2014
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K142184 · Agfa Healthcare N.V. · Oct 2014
FDR D-EVO FLAT PANEL DETECTOR SYSTEM
K141765 · Fujifilm Medical Systems U.S.A, Inc. · Oct 2014
AERODR SYSTEM 2
K141271 · Konica Minolta, Inc. · Sep 2014
DX-D IMAGING PACKAGE
K141602 · Agfa Healthcare N.V. · Sep 2014