510(k) · Cleared
ClearedVIDAvision
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vida Diagnostics, Inc. · JAK System, X-Ray, Tomography, Computed
Cleared on Aug 7, 2020 as substantially equivalent to K083227 (Vida Diagnostics, Inc., 2008) after a 114-day review. Its family tree reaches back 7 generations to 1995. 2 later devices descend from it.
- Decided
- Aug 7, 2020
- Review
- 114 days
- Class
- Class II
- Product code
- JAK
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 7 generations to K954355 (1995). 11 ancestors in all. 2 later devices descend from it, 1 citing it directly.
- Root · 7 generations backK954355 Advantage Windows 3D with Navigator OptionGeneral Electric Co. · 1995
- 6 generations backK974715 Advantage 3D XRGE Medical Systems · 1998
- 5 generations backK984634 3D-AngioSiemens Medical Corp. · 1999
- 4 generations backK011447 IN Space 3DSiemens Medical Solutions USA, Inc. · 2001
- 3 generations backK043469 Syngo Inspace 4DSiemens AG Medical Solutions · 2005
- 2 generations backK071513 Inspace 4D Software Package with Extended FunctionalitySiemens Medical Solutions · 2007
- 1 generation backK083227 Vida Pulmonary Workstation 2 (PW2)Vida Diagnostics, Inc. · 2008
- This deviceK200990 VIDAvisionVida Diagnostics, Inc. · 2020
- Descendant · cites it directly · 1 of its ownK233875 Brainomix 360 e-LungBrainomix Limited · 2024
- Descendant · 2 generations on · 0 of its ownK242411 Brainomix 360 e-LungBrainomix Limited · 2025
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −7 | K954355 | Advantage Windows 3D with Navigator Option | General Electric Co. | 1995 | — |
| −6 | K974715 | Advantage 3D XR | GE Medical Systems | 1998 | — |
| −5 | K984634 | 3D-Angio | Siemens Medical Corp. | 1999 | — |
| −4 | K011447 | IN Space 3D | Siemens Medical Solutions USA, Inc. | 2001 | — |
| −3 | K043469 | Syngo Inspace 4D | Siemens AG Medical Solutions | 2005 | — |
| −2 | K071513 | Inspace 4D Software Package with Extended Functionality | Siemens Medical Solutions | 2007 | — |
| −1 | K083227 | Vida Pulmonary Workstation 2 (PW2) | Vida Diagnostics, Inc. | 2008 | — |
| 0 (this device) | K200990 | VIDAvision | Vida Diagnostics, Inc. | 2020 | — |
| +1 | K233875 | Brainomix 360 e-Lung | Brainomix Limited | 2024 | — |
| +2 | K242411 | Brainomix 360 e-Lung | Brainomix Limited | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 1998 | 2 | 0 |
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2024 | 1 | 0 |
| 2025 | 1 | 0 |
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 JAK? 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 JAK device
- #1 K230223 iCAC Devicescore 23.5 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K083227 | Vida Pulmonary Workstation 2 (PW2)Summary page 4…Regulatory Class: Class II Regulation Description: Computed tomography x-ray system Submission Number: K083227 www.vidalung.ai VIDA Diagnostics, Inc. Traditional 510(k)… | 2008 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K233875 | Brainomix 360 e-Lung | 2024 | 1 |
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 25 years and passes through 7 companies; a new generation was cleared every 2.4 years on median.
- 1 of the 11 ancestors has a recall of any class.
- Of its descendants, K233875 (Brainomix Limited, 2024) has gone furthest, with 1 descendant of its own.
- 11 other devices also cite its predicate K083227.
How does its category compare?
All JAK devicesJAK System, X-Ray, Tomography, Computed: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.
FDA decisions per year · JAK
27in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JAK
141in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JAK
17in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JAK
219in 2025
MAUDE reports naming product code JAK, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 14 | 27 | 11 | 76 |
| 2008 | 26 | 42 | 16 | 120 |
| 2009 | 15 | 31 | 29 | 105 |
| 2010 | 7 | 92 | 51 | 119 |
| 2011 | 16 | 155 | 34 | 205 |
| 2012 | 28 | 121 | 23 | 192 |
| 2013 | 17 | 132 | 11 | 414 |
| 2014 | 30 | 200 | 10 | 308 |
| 2015 | 30 | 140 | 28 | 454 |
| 2016 | 25 | 129 | 44 | 365 |
| 2017 | 29 | 96 | 33 | 338 |
| 2018 | 24 | 114 | 10 | 543 |
| 2019 | 28 | 94 | 5 | 233 |
| 2020 | 30 | 112 | 8 | 177 |
| 2021 | 20 | 145 | 15 | 261 |
| 2022 | 30 | 131 | 9 | 199 |
| 2023 | 27 | 139 | 9 | 310 |
| 2024 | 26 | 141 | 20 | 212 |
| 2025 | 27 | 141 | 17 | 219 |
| 2026 | 21 | 167 | 23 | — |
What is it indicated for?
The VIDA|vision software provides reproducible CT values for pulmonary tissue, which is essential for providing quantitative support for diagnosis and follow up examinations. VIDA|vision can be used to support the physician in the diagnosis and documentation of pulmonary tissue images (e.g., abnormalities) from CT thoracic datasets. Three-D segmentation and isolation of sub-compartments, volumetric analysis, density evaluations, low density cluster…
Read the full statement (104 words)
The VIDA|vision software provides reproducible CT values for pulmonary tissue, which is essential for providing quantitative support for diagnosis and follow up examinations. VIDA|vision can be used to support the physician in the diagnosis and documentation of pulmonary tissue images (e.g., abnormalities) from CT thoracic datasets. Three-D segmentation and isolation of sub-compartments, volumetric analysis, density evaluations, low density cluster analysis and reporting tools are combined with a dedicated workflow. The VIDA|vision software package is also intended to be a real-time interactive evaluation in space and time for CT volume data sets that provides the reconstruction of two dimensional images into a three-dimensional image format.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K200990 · printed Nov 6, 2026
Cite this page
510(k) Report. “K200990: VIDAvision.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200990
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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