Cleared Traditional

QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT (K140342) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K140342 · Mindways Software, Inc. · Radiology device
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Aug 2014
Decision
199d
Days
Class 2
Risk

K140342 is an FDA 510(k) clearance for the QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT. Classified as Densitometer, Bone (product code KGI), Class II - Special Controls.

Submitted by Mindways Software, Inc. (Austin, US). The FDA issued a Cleared decision on August 29, 2014 after a review of 199 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1170 - 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 Mindways Software, Inc. devices

Submission Details

510(k) Number K140342 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 11, 2014
Decision Date August 29, 2014
Days to Decision 199 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
92d slower than avg
Panel avg: 107d · This submission: 199d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KGI Densitometer, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1170
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 - KGI Densitometer, Bone

All 11
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