Cleared Abbreviated

K000474 - VIEW NT

K000474 is the FDA 510(k) clearance for VIEW NT by Electromed Intl., Ltd.. It is a Class 2 Radiology device (product code LLZ) cleared through the Abbreviated 510(k) pathway after a 65-day FDA review.

K000474 · Electromed Intl., Ltd. · Radiology device
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Apr 2000
Decision
65d
Days
Class 2
Risk

K000474 is an FDA 510(k) clearance for the VIEW NT. 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 Electromed Intl., Ltd. (St-Eustache, Quebec, CA). The FDA issued a Cleared decision on April 19, 2000 after a review of 65 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 Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Incremental AI imaging tool. Standards-verified equivalence. 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 Electromed Intl., Ltd. devices

Submission Details

510(k) Number K000474 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 14, 2000
Decision Date April 19, 2000
Days to Decision 65 days
Submission Type Abbreviated
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 107d · This submission: 65d
Pathway characteristics
Standards-based clearance path.

Device Classification

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 1136
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