Cleared Traditional

K003762 - ALI 3D TOOL MODULE FOR MEDICAL IMAGES

K003762 is an FDA 510(k) clearance for ALI 3D TOOL MODULE FOR MEDICAL IMAGES, manufactured by A.L.I. Technologies, Inc.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K003762 · A.L.I. Technologies, Inc. · Radiology device
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Feb 2001
Decision
84d
Days
Class 2
Risk

K003762 is an FDA 510(k) clearance for the ALI 3D TOOL MODULE FOR MEDICAL IMAGES. Classified as System, Image Processing, Radiological within the LLZ classification (a category encompassing advanced image processing and PACS-adjacent software), Class II - Special Controls.

Submitted by A.L.I. Technologies, Inc. (Richmond, B.C., CA). The FDA issued a Cleared decision on February 28, 2001 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2050 - 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: Incremental AI imaging tool. Moderate equivalence dependency. Overall, this clearance reflects a predicate-aligned approval typical of modern AI radiology extensions - not a novel clinical breakthrough, but a validated iteration within an established regulatory category.

View all A.L.I. Technologies, Inc. devices

FDA 510(k) Submission Details - K003762

510(k) Number K003762 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 06, 2000
Decision Date February 28, 2001
Days to Decision 84 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
23d faster than avg
Panel avg: 107d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LLZ Device Classification - Class 2, Special Controls

Product Code LLZ System, Image Processing, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2050
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 - LLZ System, Image Processing, Radiological

All 1717
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