Cleared Traditional

K130224 - ICT

K130224 is an FDA 510(k) clearance for ICT, manufactured by Imris, Inc.. The device is a Class 2 Radiology device with product code JAK cleared through the Traditional 510(k) pathway after a 170-day FDA review.

K130224 · Imris, Inc. · Radiology device
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Jul 2013
Decision
170d
Days
Class 2
Risk

K130224 is an FDA 510(k) clearance for the ICT. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Imris, Inc. (Winnipeg, Mb, CA). The FDA issued a Cleared decision on July 18, 2013 after a review of 170 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - 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 Imris, Inc. devices

FDA 510(k) Submission Details - K130224

510(k) Number K130224 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 2013
Decision Date July 18, 2013
Days to Decision 170 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
63d slower than avg
Panel avg: 107d · This submission: 170d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAK Device Classification - Class 2, Special Controls

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
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 - JAK System, X-ray, Tomography, Computed

All 646
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K130224.
SYNGO CT PULMO 3D
K123540 · Siemens Medical Systems, Inc. · Aug 2013
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K130960 · Toshibamedical Systems Corporation · Aug 2013
PERCUNAV SYSTEM
K132087 · Philips Health Care · Jul 2013
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K130645 · Toshibamedical Systems Corporation · Jun 2013
AQUILION LB TRITON V4.91
K123500 · Toshibamedical Systems Corporation · May 2013
SYNGO.CT NEURO PERFUSION
K123541 · Siemens Medical Systems, Inc. · Apr 2013