510(k) Report

510(k) · Cleared

Cleared

ADAS 3D

K240791510(k) TraditionalCleared Sep 9, 2024171-day reviewClass II21 CFR 892.2050

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Adas3D Medical S.L. · QIH Automated Radiological Image Processing Software

Cleared on Sep 9, 2024 as substantially equivalent to K230803 (Adas3D Medical S.L., 2023) after a 171-day review. Its family tree reaches back 10 generations to 1994. 1 later device descends from it.

Decided
Sep 9, 2024
Review
171 days
Class
Class II
Product code
QIH
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K940172 (1994). 23 ancestors in all, the oldest K871859 (1987). 1 later device descends from it, 1 citing it directly.

  1. Root · 10 generations backK940172 Cardiovascular Measurement System-CMSMedis Medical Imaging Systems, Inc. · 1994
  2. 6 generations between
  3. 3 generations backK210850 ADAS 3DAdas3D Medical S.L. · 2021
  4. 2 generations backK212421 ADAS 3DAdas3D Medical S.L. · 2021
  5. 1 generation backK230803 ADAS 3DAdas3D Medical S.L. · 2023
  6. This deviceK240791 ADAS 3DAdas3D Medical S.L. · 2024
  7. Descendant · cites it directly · 0 of its ownK253969 ADAS 3DAdas3D Medical S.L. · 2026
Show all 10 generations
  1. Root · 10 generations backK940172 Cardiovascular Measurement System-CMSMedis Medical Imaging Systems, Inc. · 1994
  2. 9 generations backK993765 Quantitative Analysis of Left Ventricular Angiograms (QLV)Medis Medical Imaging Systems BV · 1999
  3. 8 generations backK994283 Mri- Magnetic Resonance Analytical Software SystemMedis Medical Imaging Systems BV · 2000
  4. 7 generations backK031927 GE Delta Software Option for MriGE Medical Systems · 2003
  5. 6 generations backK121762 Cardiac VXGe Medical Systems, LLC · 2013 · Recalled
  6. 5 generations backK140587 MR-CT VvaMedis Medical Imaging Systems BV · 2015
  7. 4 generations backK191125 ADAS 3DGalgo Medical S.L · 2020
  8. 3 generations backK210850 ADAS 3DAdas3D Medical S.L. · 2021
  9. 2 generations backK212421 ADAS 3DAdas3D Medical S.L. · 2021
  10. 1 generation backK230803 ADAS 3DAdas3D Medical S.L. · 2023
  11. This deviceK240791 ADAS 3DAdas3D Medical S.L. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K253969ADAS 3DAdas3D Medical S.L. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K940172Cardiovascular Measurement System-CMSMedis Medical Imaging Systems, Inc.1994—
−9K993765Quantitative Analysis of Left Ventricular Angiograms (QLV)Medis Medical Imaging Systems BV1999—
−8K994283Mri- Magnetic Resonance Analytical Software SystemMedis Medical Imaging Systems BV2000—
−7K031927GE Delta Software Option for MriGE Medical Systems2003—
−6K121762Cardiac VXGe Medical Systems, LLC20131
−5K140587MR-CT VvaMedis Medical Imaging Systems BV2015—
−4K191125ADAS 3DGalgo Medical S.L2020—
−3K210850ADAS 3DAdas3D Medical S.L.2021—
−2K212421ADAS 3DAdas3D Medical S.L.2021—
−1K230803ADAS 3DAdas3D Medical S.L.2023—
0 (this device)K240791ADAS 3DAdas3D Medical S.L.2024—
+1K253969ADAS 3DAdas3D Medical S.L.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199120
199320
199510
199610
199710
200010
200110
200410
200810
201110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K240791, 1994–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in QIH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new QIH device

  1. #1 K213998 cvi42 Auto Imaging Software Applicationscore 23.6 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K230803ADAS 3D
Summary page 5
…Secondary product code: LLZ REGULATION DESCRIPTION: Picture archiving and communications system PREDICATE DEVICE: ADAS 3D (K230803) 09-09-2024 510(k) Summary K240791 2 Device Description…
Adas3D Medical S.L.2023—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K253969ADAS 3DAdas3D Medical S.L.20260

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 30 years and passes through 6 companies; a new generation was cleared every 2.0 years on median.
  • 6 of the 23 ancestors have a recall of any class.
  • Of its descendants, K253969 (Adas3D Medical S.L., 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All QIH devices

QIH Automated Radiological Image Processing Software: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · QIH

94in 2025

2019: 22020: 112021: 192022: 252023: 452024: 642025: 942026 (partial year): 78
2007high 94 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QIH

150in 2025

2020: 145 days median2021: 125 days median2022: 134 days median2023: 151 days median2024: 141 days median2025: 150 days median2026 (partial year): 130 days median
2007high 151 (2023) · low 125 (2021)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · QIH

1so far in 2026, the most since 2007

2026 (partial year): 1
2007high 1 (2026) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · QIH

4in 2025

2024: 22025: 4
2007high 4 (2025) · low 0 (2007)2025

MAUDE reports naming product code QIH, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20192—00
20201114500
20211912500
20222513400
20234515100
20246414102
20259415004
2026781301—

What is it indicated for?

ADAS 3D is indicated for use in clinical settings to support the visualization and analysis of MR and CT images of the heart for use on individual patients with cardiovascular disease. ADAS 3D is indicated for patients with myocardial scar produced by ischemic or non-ischemic heart disease. ADAS 3D processes MR and CT images. The quality and the resolution of the medical images determines the accuracy of the data produced by ADAS 3D. ADAS 3D is indicated…

Read the full statement (184 words)

ADAS 3D is indicated for use in clinical settings to support the visualization and analysis of MR and CT images of the heart for use on individual patients with cardiovascular disease.

ADAS 3D is indicated for patients with myocardial scar produced by ischemic or non-ischemic heart disease. ADAS 3D processes MR and CT images. The quality and the resolution of the medical images determines the accuracy of the data produced by ADAS 3D.

ADAS 3D is indicated to be used only by qualified medical professionals (cardiologists, electrophysiologists, radiologists or trained technicians) for the calculation, quantification and visualization of cardiac images and intended to be used for pre-planning and during electrophysiology procedures. The data produced by ADAS 3D must not be used as an irrefutable basis or a source of medical advice for clinical diagnosis or patient treatment. The data produced by ADAS 3D is intended to be used to support qualified medical professionals for clinical decision making.

The clinical significance of using ADAS 3D to identify arrhythmia substrates for the treatment of cardiac arrhythmias (e.g., ventricular tachycardia) or risk stratification has not been established.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K240791: ADAS 3D.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K240791

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026