Cleared Traditional

K954678 - PRO VISION

K954678 is an FDA 510(k) clearance for PRO VISION, manufactured by Algotec Systems, Ltd.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 87-day FDA review.

K954678 · Algotec Systems, Ltd. · Radiology device
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Jan 1996
Decision
87d
Days
Class 2
Risk

K954678 is an FDA 510(k) clearance for the PRO VISION. 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 Algotec Systems, Ltd. (Efrat, IL). The FDA issued a Cleared decision on January 5, 1996 after a review of 87 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 Algotec Systems, Ltd. devices

FDA 510(k) Submission Details - K954678

510(k) Number K954678 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 10, 1995
Decision Date January 05, 1996
Days to Decision 87 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
20d faster than avg
Panel avg: 107d · This submission: 87d
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 1330
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K954678.
DIGISCAN 2 PLUS
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GE ADVANTAGE DICOM CR REPROCESSING STATION
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K944612 · Codman & Shurtleff, Inc. · Dec 1995
VOXELVIEW
K953259 · Vital Images, Inc. · Nov 1995