Cleared Special

K142698 - PerkinElmer

K142698 is an FDA 510(k) clearance for PerkinElmer, manufactured by Perkinelmer, Inc.. The device is a Class 2 Radiology device with product code MQB cleared through the Special 510(k) pathway after a 31-day FDA review.

K142698 · Perkinelmer, Inc. · Radiology device
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Oct 2014
Decision
31d
Days
Class 2
Risk

K142698 is an FDA 510(k) clearance for the PerkinElmer, XRpad 4343 F MED Flat Panel Detector. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Perkinelmer, Inc. (Waltham, US). The FDA issued a Cleared decision on October 23, 2014 after a review of 31 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. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Perkinelmer, Inc. devices

FDA 510(k) Submission Details - K142698

510(k) Number K142698 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 2014
Decision Date October 23, 2014
Days to Decision 31 days
Submission Type Special
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 107d · This submission: 31d
Pathway characteristics
Modification to existing cleared device.

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 260
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K142698.
1717SGN / 1717SCN Digital Flat Panel X-ray Detector
K150150 · Rayence Co., Ltd. · Mar 2015
RIS500
K143000 · Ray Co., Ltd. · Jan 2015
EVS 4343
K142475 · DRTECH Corporation · Jan 2015
FDR D-EVO II FLAT PANEL DETECTOR SYSTEM
K142003 · Fujifilm Medical System U.S.A., Inc. · Oct 2014
DX-D IMAGING PACKAGE
K142184 · Agfa Healthcare N.V. · Oct 2014
FDR D-EVO FLAT PANEL DETECTOR SYSTEM
K141765 · Fujifilm Medical Systems U.S.A, Inc. · Oct 2014