Cleared Abbreviated

K120514 - CARDIOPACS

K120514 is an FDA 510(k) clearance for CARDIOPACS, manufactured by Lumedx. The device is a Class 2 Radiology device with product code LLZ cleared through the Abbreviated 510(k) pathway after a 135-day FDA review.

K120514 · Lumedx · Radiology device
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Jul 2012
Decision
135d
Days
Class 2
Risk

K120514 is an FDA 510(k) clearance for the CARDIOPACS. 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 Lumedx (Bellevue, US). The FDA issued a Cleared decision on July 5, 2012 after a review of 135 days - within the typical 510(k) review window.

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 Lumedx devices

FDA 510(k) Submission Details - K120514

510(k) Number K120514 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 21, 2012
Decision Date July 05, 2012
Days to Decision 135 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
28d slower than avg
Panel avg: 107d · This submission: 135d
Pathway characteristics
Standards-based clearance path.

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 1204
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K120514.
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K120472 · Hologic, Inc. · Jun 2012
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K121459 · Siemens Medical Solutions USA, Inc. · Jun 2012