Cleared Traditional

K012093 - AETMED IMAGE PROCESSING SOFTWARE

K012093 is an FDA 510(k) clearance for AETMED IMAGE PROCESSING SOFTWARE, manufactured by Aetmed, S.P.A.. The device is a Class 2 Radiology device with product code LLZ cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K012093 · Aetmed, S.P.A. · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Sep 2001
Decision
78d
Days
Class 2
Risk

K012093 is an FDA 510(k) clearance for the AETMED IMAGE PROCESSING SOFTWARE. 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 Aetmed, S.P.A. (Indianpolis, US). The FDA issued a Cleared decision on September 21, 2001 after a review of 78 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.

FDA 510(k) Submission Details - K012093

510(k) Number K012093 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 2001
Decision Date September 21, 2001
Days to Decision 78 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
29d faster than avg
Panel avg: 107d · This submission: 78d
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 2293
Devices cleared under the same product code (LLZ) and FDA review panel - the closest regulatory comparables to K012093.
ICONNECTION 3D
K012779 · Hinnovation, Inc. · Nov 2001
CAAS II QVA
K012475 · Pie Medical Imaging BV · Oct 2001
RAPIDIA
K012290 · 3D Med Co., Ltd. · Sep 2001
AQUARIUSNET SERVER
K012086 · Terarecon,Inc. · Sep 2001
VIEWSTATION
K011694 · Impac Medical Systems, Inc. · Aug 2001
KODAK RADIATION ONCOLOGY SOFTWARE/ FOR ACR SYSTEMS
K012155 · Eastman Kodak Company · Aug 2001
K012093 · AETMED IMAGE PROCESSING SOFTWARE
Download PDF FDA Summary Aetmed, S.P.A.