Cleared Traditional

K142475 - EVS 4343

K142475 is an FDA 510(k) clearance for EVS 4343, manufactured by DRTECH Corporation. The device is a Class 2 Radiology device with product code MQB cleared through the Traditional 510(k) pathway after a 134-day FDA review.

K142475 · DRTECH Corporation · Radiology device
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Jan 2015
Decision
134d
Days
Class 2
Risk

K142475 is an FDA 510(k) clearance for the EVS 4343. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by DRTECH Corporation (Seongam-Si, KR). The FDA issued a Cleared decision on January 15, 2015 after a review of 134 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 DRTECH Corporation devices

FDA 510(k) Submission Details - K142475

510(k) Number K142475 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 03, 2014
Decision Date January 15, 2015
Days to Decision 134 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
27d slower than avg
Panel avg: 107d · This submission: 134d
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 259
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K142475.
Carestream DRX-1 System
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RIS500
K143000 · Ray Co., Ltd. · 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