Cleared Special

K060550 - KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80...

K060550 is the FDA 510(k) clearance for KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80... by Eastman Kodak Company. It is a Class 2 Radiology device (product code KPR) cleared through the Special 510(k) pathway after a 29-day FDA review.

K060550 · Eastman Kodak Company · Radiology device
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Optimized for regulatory review, auditing and printing
Mar 2006
Decision
29d
Days
Class 2
Risk

K060550 is an FDA 510(k) clearance for the KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Eastman Kodak Company (Rochester, US). The FDA issued a Cleared decision on March 31, 2006 after a review of 29 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 Eastman Kodak Company devices

Submission Details

510(k) Number K060550 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 02, 2006
Decision Date March 31, 2006
Days to Decision 29 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
78d faster than avg
Panel avg: 107d · This submission: 29d
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 K060550.
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KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345
K051258 · Eastman Kodak Company · Jun 2005
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K050704 · General Electric Co. · Apr 2005