Cleared Traditional

K142184 - DX-D IMAGING PACKAGE

K142184 is an FDA 510(k) clearance for DX-D IMAGING PACKAGE, manufactured by Agfa Healthcare N.V.. The device is a Class 2 Radiology device with product code MQB cleared through the Traditional 510(k) pathway after a 69-day FDA review.

K142184 · Agfa Healthcare N.V. · Radiology device
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Oct 2014
Decision
69d
Days
Class 2
Risk

K142184 is an FDA 510(k) clearance for the DX-D IMAGING PACKAGE. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Agfa Healthcare N.V. (Greenville, US). The FDA issued a Cleared decision on October 16, 2014 after a review of 69 days - a notably fast clearance cycle.

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: 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 Agfa Healthcare N.V. devices

FDA 510(k) Submission Details - K142184

510(k) Number K142184 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 08, 2014
Decision Date October 16, 2014
Days to Decision 69 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
38d faster than avg
Panel avg: 107d · This submission: 69d
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 244
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K142184.
Carestream DRX-1 System
K150766 · Carestream Health, Inc. · Jun 2015
1717SGN / 1717SCN Digital Flat Panel X-ray Detector
K150150 · Rayence Co., Ltd. · Mar 2015
FDR D-EVO II FLAT PANEL DETECTOR SYSTEM
K142003 · Fujifilm Medical System U.S.A., Inc. · Oct 2014
FDR D-EVO FLAT PANEL DETECTOR SYSTEM
K141765 · Fujifilm Medical Systems U.S.A, Inc. · Oct 2014
DX-D IMAGING PACKAGE
K141602 · Agfa Healthcare N.V. · Sep 2014
SOLID STATE X-RAY IMAGING DEVICE, DIGITAL FLAT PANEL X-RAY DETECTOR, 1417WGC
K141563 · Rayence Co., Ltd. · Jul 2014