Cleared Traditional

K113449 - FUSION FLAT PANEL

K113449 is an FDA 510(k) clearance for FUSION FLAT PANEL, manufactured by Icrco, Inc.. The device is a Class 2 Radiology device with product code MQB cleared through the Traditional 510(k) pathway after a 206-day FDA review.

K113449 · Icrco, Inc. · Radiology device
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Jun 2012
Decision
206d
Days
Class 2
Risk

K113449 is an FDA 510(k) clearance for the FUSION FLAT PANEL. Classified as Solid State X-ray Imager (flat Panel/digital Imager) (product code MQB), Class II - Special Controls.

Submitted by Icrco, Inc. (Torrance, US). The FDA issued a Cleared decision on June 14, 2012 after a review of 206 days - an extended review 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: 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 Icrco, Inc. devices

FDA 510(k) Submission Details - K113449

510(k) Number K113449 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 2011
Decision Date June 14, 2012
Days to Decision 206 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
99d slower than avg
Panel avg: 107d · This submission: 206d
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 289
Devices cleared under the same product code (MQB) and FDA review panel - the closest regulatory comparables to K113449.
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K120131 · Konica Minolta Medical & Graphic, Inc. · Feb 2012