510(k) Report

510(k) · Cleared

Cleared

DASI Dimensions (V1.0)

K231324510(k) TraditionalCleared Jan 8, 2024245-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

Dasi Simulations · QIH Automated Radiological Image Processing Software

Cleared on Jan 8, 2024 as substantially equivalent to K153736 (Pie Medical Imaging BV, 2016) after a 245-day review. Its family tree reaches back 7 generations to 1996.

Decided
Jan 8, 2024
Review
245 days
Class
Class II
Product code
QIH
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K954678 (1996). 19 ancestors in all, the oldest K954668 (1995). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2015: 1 other ancestor2006: 2 other ancestors2004: 2 other ancestors2002: 1 other ancestor2000: 1 other ancestor1995: 1 other ancestor2001: 1 other ancestor1997: 1 other ancestor1996: 2 other ancestorsK954678 · Pro Vision · Algotec Systems, Ltd. · 1996K980648 · Pro Vision · Algotec Systems, Ltd. · 1998K992654 · Plug 'N View 3D, Version 1.0 · Voxar Limited · 1999K043097 · 3VISEON · 3Mensio Medical Imaging BV · 2004K072653 · 3VISEON/Surgery · 3Mensio Medical Imaging BV · 2008K120367 · 3MENSIO Workstation · Pie Medical Imaging BV · 2012K153736 · 3mensio Workstation · Pie Medical Imaging BV · 2016 · recalled1995200020052010201520202025
Other ancestors, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor4 generations back: 3 other ancestors5 generations back: 3 other ancestors6 generations back: 2 other ancestors7 generations back: 2 other ancestors K153736 · 3mensio Workstation · Pie Medical Imaging BV · 2016 · recalledK120367 · 3MENSIO Workstation · Pie Medical Imaging BV · 2012K072653 · 3VISEON/Surgery · 3Mensio Medical Imaging BV · 2008K043097 · 3VISEON · 3Mensio Medical Imaging BV · 2004K992654 · Plug 'N View 3D, Version 1.0 · Voxar Limited · 1999K980648 · Pro Vision · Algotec Systems, Ltd. · 1998K954678 · Pro Vision · Algotec Systems, Ltd. · 1996−50
  1. Root · 7 generations backK954678 Pro VisionAlgotec Systems, Ltd. · 1996
  2. 6 generations backK980648 Pro VisionAlgotec Systems, Ltd. · 1998
  3. 5 generations backK992654 Plug 'N View 3D, Version 1.0Voxar Limited · 1999
  4. 4 generations backK043097 3VISEON3Mensio Medical Imaging BV · 2004
  5. 3 generations backK072653 3VISEON/Surgery3Mensio Medical Imaging BV · 2008
  6. 2 generations backK120367 3MENSIO WorkstationPie Medical Imaging BV · 2012
  7. 1 generation backK153736 3mensio WorkstationPie Medical Imaging BV · 2016 · Recalled
  8. This deviceK231324 DASI Dimensions (V1.0)Dasi Simulations · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K954678Pro VisionAlgotec Systems, Ltd.1996—
−6K980648Pro VisionAlgotec Systems, Ltd.1998—
−5K992654Plug 'N View 3D, Version 1.0Voxar Limited1999—
−4K0430973VISEON3Mensio Medical Imaging BV2004—
−3K0726533VISEON/Surgery3Mensio Medical Imaging BV2008—
−2K1203673MENSIO WorkstationPie Medical Imaging BV2012—
−1K1537363mensio WorkstationPie Medical Imaging BV20161
0 (this device)K231324DASI Dimensions (V1.0)Dasi Simulations2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199620
199710
200010
200110
200210
200420
200620
201510
FIG. 1 — Lineage of K231324, 1996–2024Source: 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 23.5 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K1537363mensio Workstation
Summary page 4
…21 CFR 807.92(a)(3) Predicate# Predicate Trade Name (Primary Predicate is listed first) Product Code I K153736 I I 3mensio Workstation 1 1 LLZ Device Descr…
Pie Medical Imaging BV20161

Also cleared against K153736: 10 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 28 years and passes through 5 companies; a new generation was cleared every 4.1 years on median.
  • 5 of the 19 ancestors have a recall of any class.
  • 10 other devices also cite its predicate K153736.

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?

DASI Dimensions is a standalone, non-invasive, clinical decision support software solution that is intended for use by cardiologists and radiologists in context of the aortic stenosis population.

DASI Dimensions provides the end-user with pre-defined images and measurements (diameters, lengths, angles, areas, and perimeters) of cardiovascular structures.

The clinician receiving the results retains the responsibility for interpreting and validating all information and making all patient treatment decisions.

DASI Dimensions is not intended to replace the clinician's decision or device's instructions for use.

DASI Dimensions is prescription use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231324: DASI Dimensions (V1.0).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231324

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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