510(k) · Cleared
ClearedDeep Learning Image Reconstruction
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ge Healthcare Japan Corporation · JAK System, X-Ray, Tomography, Computed
Cleared on Sep 17, 2021 as substantially equivalent to K193170 (Ge Healthcare Japan Corporation, 2019) after a 77-day review. Its family tree reaches back 10 generations to 2001.
- Decided
- Sep 17, 2021
- Review
- 77 days
- Class
- Class II
- Product code
- JAK
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 10 generations to K013561 (2001). 15 ancestors in all. No later device cites it as a predicate yet.
- Root · 10 generations backK013561 Lightspeed 4.0 CT Scanner SystemGE Medical Systems · 2001 · Recalled
- 6 generations between
- 3 generations backK163213 Revolution CTGe Medical Systems, LLC · 2016 · Recalled
- 2 generations backK183202 Deep Learning Image ReconstructionGe Medical Systems, LLC · 2019
- 1 generation backK193170 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2019
- This deviceK212067 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2021
Show all 10 generations
- Root · 10 generations backK013561 Lightspeed 4.0 CT Scanner SystemGE Medical Systems · 2001 · Recalled
- 9 generations backK030420 Lightspeed 5.0 Computed Tomography SystemGE Medical Systems · 2003 · Recalled
- 8 generations backK040372 Lightspeed 7.0 CT Scanner SystemGe Medical Systems, LLC · 2004 · Recalled
- 7 generations backK061817 Lightspeed 7.1 CT Scanner SystemGe Medical Systems, LLC · 2006 · Recalled
- 6 generations backK081105 GE Lightspeed CT750 HD (Lightspeed 8.0)GE Healthcare · 2008 · Recalled
- 5 generations backK120833 Discovery CT750 HDGe Medical Systems, LLC · 2012 · Recalled
- 4 generations backK133705 Revolution CTGe Medical Systems, LLC · 2014 · Recalled
- 3 generations backK163213 Revolution CTGe Medical Systems, LLC · 2016 · Recalled
- 2 generations backK183202 Deep Learning Image ReconstructionGe Medical Systems, LLC · 2019
- 1 generation backK193170 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2019
- This deviceK212067 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K013561 | Lightspeed 4.0 CT Scanner System | GE Medical Systems | 2001 | 5 |
| −9 | K030420 | Lightspeed 5.0 Computed Tomography System | GE Medical Systems | 2003 | 4 |
| −8 | K040372 | Lightspeed 7.0 CT Scanner System | Ge Medical Systems, LLC | 2004 | 5 |
| −7 | K061817 | Lightspeed 7.1 CT Scanner System | Ge Medical Systems, LLC | 2006 | 1 |
| −6 | K081105 | GE Lightspeed CT750 HD (Lightspeed 8.0) | GE Healthcare | 2008 | 5 |
| −5 | K120833 | Discovery CT750 HD | Ge Medical Systems, LLC | 2012 | 1 |
| −4 | K133705 | Revolution CT | Ge Medical Systems, LLC | 2014 | 14 |
| −3 | K163213 | Revolution CT | Ge Medical Systems, LLC | 2016 | 16 |
| −2 | K183202 | Deep Learning Image Reconstruction | Ge Medical Systems, LLC | 2019 | — |
| −1 | K193170 | Deep Learning Image Reconstruction | Ge Healthcare Japan Corporation | 2019 | — |
| 0 (this device) | K212067 | Deep Learning Image Reconstruction | Ge Healthcare Japan Corporation | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2008 | 1 | 0 |
| 2011 | 2 | 0 |
| 2014 | 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 |
|---|---|---|---|
| * | K193170 | Deep Learning Image ReconstructionSummary page 4…edicate Device Information Device Name: Deep Learning Image Reconstruction Manufacturer: GE Medical Systems, LLC 510(k) Number: K193170 cleared on December 13, 2019 Regulation Number/ 21 CFR 892.1750 Computed tomography x-ray system / JAK Product Code:… | 2019 |
| † | K133640 | ASIR-V | 2014 |
| † | K203169 | Revolution Ascend | 2020 |
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 20 years and passes through 4 companies; a new generation was cleared every 1.8 years on median.
- 11 of the 15 ancestors have a recall of any class.
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. 2021, 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 Deep Learning Image Reconstruction software is a deep learning based reconstruction method intended to produce cross-sectional images of the head and whole body by computer reconstruction of X-ray transmission data taken at different angles and planes, including Axial, Helical (Volumetric), and Cardiac acquisitions, for all ages.
Deep Learning Image Reconstruction software can be used for head, whole body, cardiac, and vascular CT applications.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K212067 · printed Nov 4, 2026
Cite this page
510(k) Report. “K212067: Deep Learning Image Reconstruction.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K212067
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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