510(k) · Cleared
ClearedSCENARIA View Phase 6.0
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Fujifilm Corporation · JAK System, X-Ray, Tomography, Computed
Cleared on Sep 18, 2026 as substantially equivalent to K250370 (Fujifilm Corporation, 2025) after a 156-day review. Its family tree reaches back 14 generations to 2003.
- Decided
- Sep 18, 2026
- Review
- 156 days
- Class
- Class II
- Product code
- JAK
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 14 generations to K031469 (2003). 15 ancestors in all. No later device cites it as a predicate yet.
- Root · 14 generations backK031469 Aquilion Super 4 Multislice CT Scanner, Model TSX-101A/7Toshiba America Medical Systems, In.C · 2003 · Recalled
- 10 generations between
- 3 generations backK213829 SCENARIA ViewFujifilm Healthcare Corporation · 2022 · Recalled
- 2 generations backK231574 Scenaria View 4.2FUJIFILM Healthcare Americas Corporation · 2023
- 1 generation backK250370 SCENARIA View Phase 5.0Fujifilm Corporation · 2025
- This deviceK261229 SCENARIA View Phase 6.0Fujifilm Corporation · 2026
Show all 14 generations
- Root · 14 generations backK031469 Aquilion Super 4 Multislice CT Scanner, Model TSX-101A/7Toshiba America Medical Systems, In.C · 2003 · Recalled
- 13 generations backK033418 TSX-101A/a and TSX-101A/C Aquilion Multislice CT ScannersToshiba America Medical Systems, In.C · 2003 · Recalled
- 12 generations backK051833 TSX-101A/H Aquilion 64 SP CT Scanner; TSX-101A/I Aquilion 32 SP CT…Toshiba America Medical Systems, In.C · 2005
- 11 generations backK080211 Model TSX-101A/H/I Aquilion 32/64 SP CT SystemToshiba America Medical Systems, In.C · 2008 · Recalled
- 10 generations backK101888 Scenaria Whole-Body X-Ray CT SystemHitachi Medical Systems America, Inc. · 2011 · Recalled
- 9 generations backK123509 Scenaria Phase 2 Whole-Body X-Ray CT SystemHitachi Medical Systems America, Inc. · 2013
- 8 generations backK161748 SUPRIA w/guideShot OptionHitachi Medical Systems America, Inc. · 2016
- 7 generations backK163528 HITACHI Supria Whole-body X-ray CT System Phase 3Hitachi Medical Systems America, Inc. · 2017
- 6 generations backK171738 Supria True64Hitachi Healthcare Americas Corporation · 2017
- 5 generations backK190841 SCENARIA ViewHitachi Healthcare Americas · 2019
- 4 generations backK200498 SCENARIA ViewHitachi Healthcare Americas · 2020
- 3 generations backK213829 SCENARIA ViewFujifilm Healthcare Corporation · 2022 · Recalled
- 2 generations backK231574 Scenaria View 4.2FUJIFILM Healthcare Americas Corporation · 2023
- 1 generation backK250370 SCENARIA View Phase 5.0Fujifilm Corporation · 2025
- This deviceK261229 SCENARIA View Phase 6.0Fujifilm Corporation · 2026
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −14 | K031469 | Aquilion Super 4 Multislice CT Scanner, Model TSX-101A/7 | Toshiba America Medical Systems, In.C | 2003 | 1 |
| −13 | K033418 | TSX-101A/a and TSX-101A/C Aquilion Multislice CT Scanners | Toshiba America Medical Systems, In.C | 2003 | 2 |
| −12 | K051833 | TSX-101A/H Aquilion 64 SP CT Scanner; TSX-101A/I Aquilion 32 SP CT Scanner | Toshiba America Medical Systems, In.C | 2005 | — |
| −11 | K080211 | Model TSX-101A/H/I Aquilion 32/64 SP CT System | Toshiba America Medical Systems, In.C | 2008 | 8 |
| −10 | K101888 | Scenaria Whole-Body X-Ray CT System | Hitachi Medical Systems America, Inc. | 2011 | 3 |
| −9 | K123509 | Scenaria Phase 2 Whole-Body X-Ray CT System | Hitachi Medical Systems America, Inc. | 2013 | — |
| −8 | K161748 | SUPRIA w/guideShot Option | Hitachi Medical Systems America, Inc. | 2016 | — |
| −7 | K163528 | HITACHI Supria Whole-body X-ray CT System Phase 3 | Hitachi Medical Systems America, Inc. | 2017 | — |
| −6 | K171738 | Supria True64 | Hitachi Healthcare Americas Corporation | 2017 | — |
| −5 | K190841 | SCENARIA View | Hitachi Healthcare Americas | 2019 | — |
| −4 | K200498 | SCENARIA View | Hitachi Healthcare Americas | 2020 | — |
| −3 | K213829 | SCENARIA View | Fujifilm Healthcare Corporation | 2022 | 1 |
| −2 | K231574 | Scenaria View 4.2 | FUJIFILM Healthcare Americas Corporation | 2023 | — |
| −1 | K250370 | SCENARIA View Phase 5.0 | Fujifilm Corporation | 2025 | — |
| 0 (this device) | K261229 | SCENARIA View Phase 6.0 | Fujifilm Corporation | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 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 |
|---|---|---|---|
| * | K250370 | SCENARIA View Phase 5.0Summary page 5…Computed Tomography X-ray System Regulation Number 892.1750 Product Code(s) JAK Predicate Device Name Predicate # K250370 Device Trade Name SCENARIA View Phase 5.0 Common Name System, x-ray, tomography, computed Classific… | 2025 |
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 23 years and passes through 7 companies; a new generation was cleared every 1.7 years on median.
- 6 of the 15 ancestors have a recall of any class.
- 1 other device also cites its predicate K250370.
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. 2026, 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 SCENARIA View system is indicated to acquire axial volumes of the whole body including the head. Images can be acquired in axial, helical, or dynamic modes. The SCENARIA View system can also be used for interventional needle guidance. Volume datasets acquired by a SCENARIA View system can be post-processed in the SCENARIA View system to provide additional information. Post-processing capabilities of the SCENARIA View software include multi-planar…
Read the full statement (322 words)
The SCENARIA View system is indicated to acquire axial volumes of the whole body including the head. Images can be acquired in axial, helical, or dynamic modes. The SCENARIA View system can also be used for interventional needle guidance. Volume datasets acquired by a SCENARIA View system can be post-processed in the SCENARIA View system to provide additional information. Post-processing capabilities of the SCENARIA View software include multi-planar reconstruction (MPR), and volume rendering. Volume datasets acquired by a SCENARIA View system can be transferred to external devices via a DICOM standard interface. The Low Dose CT Lung Cancer Screening Option for the SCENARIA View system is indicated for using low dose CT for lung cancer screening. The screening must be conducted with the established program criteria and protocols that have been approved and published by a governmental body, a professional medical society, and/or FUJIFILM Corporation.
AI/ML algorithms are used for Intelli IPV, AutoPose, AutoPositioning, DLR and Automatic Head Slice Setting.
Intelli IPV is developed using machine learning as AI technology to the iterative practical reconstruction automatically.
AutoPose is developed using deep learning as AI technology to detect landmarks or regions from a scanogram image. When using AutoPose, be sure to visually check the scan range and adjust it if necessary.
AutoPositioning is developed using deep learning as AI technology to detect the patient’s feature points. This function assists in patient positioning operations. Therefore, after completing the positioning operation, be sure to visually check the patient's positioning and the table position by using the light localizer.
DLR Focus is developed using deep learning as AI technology to reduce image noise through convolutional processing based on a model obtained by deep learning.
Automatic Head Slice Setting is developed using deep learning as AI technology to perform brain region segmentation, brain centroid calculation, and feature point extraction from head volume data.
AutoPose, AutoPositioning, DLR Focus and Automatic Head Slice Setting are for adult use only.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K261229 · printed Nov 6, 2026
Cite this page
510(k) Report. “K261229: SCENARIA View Phase 6.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K261229
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Record history
- FDA decision record loaded Oct 30, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026