Cleared Special

K091889 - DRX-EVOLUTION, MODEL VX3733-SYS

K091889 is an FDA 510(k) clearance for DRX-EVOLUTION, manufactured by Carestream Health, Inc.. The device is a Class 2 Radiology device with product code KPR cleared through the Special 510(k) pathway after a 26-day FDA review.

K091889 · Carestream Health, Inc. · Radiology device
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Jul 2009
Decision
26d
Days
Class 2
Risk

K091889 is an FDA 510(k) clearance for the DRX-EVOLUTION, MODEL VX3733-SYS. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Carestream Health, Inc. (Rochester, US). The FDA issued a Cleared decision on July 20, 2009 after a review of 26 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 Carestream Health, Inc. devices

FDA 510(k) Submission Details - K091889

510(k) Number K091889 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 2009
Decision Date July 20, 2009
Days to Decision 26 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
81d faster than avg
Panel avg: 107d · This submission: 26d
Pathway characteristics
Modification to existing cleared device.

KPR Device Classification - Class 2, Special Controls

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 269
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K091889.
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