Cleared Special

K050704 - MODIFICATION TO: REVOLUTION XR/D DIGITA...

K050704 is the FDA 510(k) clearance for MODIFICATION TO: REVOLUTION XR/D DIGITA... by General Electric Co.. It is a Class 2 Radiology device (product code KPR) cleared through the Special 510(k) pathway after a 21-day FDA review.

K050704 · General Electric Co. · Radiology device
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Apr 2005
Decision
21d
Days
Class 2
Risk

K050704 is an FDA 510(k) clearance for the MODIFICATION TO: REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM WITH IM.... Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by General Electric Co. (Milwaukee, US). The FDA issued a Cleared decision on April 8, 2005 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - 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 General Electric Co. devices

Submission Details

510(k) Number K050704 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 18, 2005
Decision Date April 08, 2005
Days to Decision 21 days
Submission Type Special
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
86d faster than avg
Panel avg: 107d · This submission: 21d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code KPR System, X-ray, Stationary
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 - KPR System, X-ray, Stationary

All 171
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K050704.
KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386
K060550 · Eastman Kodak Company · Mar 2006
REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM WITH TOMOSYNTHESIS
K051967 · Ge Healthcare · Aug 2005
KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345
K051258 · Eastman Kodak Company · Jun 2005
MULTIDIAGNOST ELEVA
K050151 · Philips Medical Systems North America, Inc. · Feb 2005
SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250
K043025 · Analogic Corp. · Nov 2004
SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150
K040995 · Analogic Corp. · May 2004