Cleared Traditional

K072659 - RAD VISION, MODELS E AND EU

K072659 is an FDA 510(k) clearance for RAD VISION, manufactured by Almana Medical Imaging. The device is a Class 2 Radiology device with product code KPR cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K072659 · Almana Medical Imaging · Radiology device
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Nov 2007
Decision
56d
Days
Class 2
Risk

K072659 is an FDA 510(k) clearance for the RAD VISION, MODELS E AND EU. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Almana Medical Imaging (Deer Field, US). The FDA issued a Cleared decision on November 15, 2007 after a review of 56 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Almana Medical Imaging devices

FDA 510(k) Submission Details - K072659

510(k) Number K072659 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 20, 2007
Decision Date November 15, 2007
Days to Decision 56 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 107d · This submission: 56d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 218
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K072659.
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K071430 · Analogic Corp. · Jun 2007
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