Cleared Special

K052260 - SUPERDIMENSION/BRONCHUS 4.1

K052260 is an FDA 510(k) clearance for SUPERDIMENSION/BRONCHUS 4.1, manufactured by Superdimension, Ltd.. The device is a Class 2 Radiology device with product code JAK cleared through the Special 510(k) pathway after a 20-day FDA review.

K052260 · Superdimension, Ltd. · Radiology device
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Sep 2005
Decision
20d
Days
Class 2
Risk

K052260 is an FDA 510(k) clearance for the SUPERDIMENSION/BRONCHUS 4.1. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Superdimension, Ltd. (Hasbrouck Heights, US). The FDA issued a Cleared decision on September 8, 2005 after a review of 20 days - a notably fast clearance cycle.

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

FDA 510(k) Submission Details - K052260

510(k) Number K052260 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 19, 2005
Decision Date September 08, 2005
Days to Decision 20 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
87d faster than avg
Panel avg: 107d · This submission: 20d
Pathway characteristics
Modification to existing cleared device.

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 654
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