510(k) · Cleared
ClearedSyngo Dual Energy
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Siemens Medical Solutions USA, Inc. · JAK System, X-Ray, Tomography, Computed
Cleared on Oct 5, 2006 as substantially equivalent to K040970 (Siemens Medical Systems, Inc., 2004) and 2 other predicates after a 55-day review. Its family tree reaches back 5 generations to 1995. 1 of the 187 devices in its family, counting itself, has a Class I recall. 169 later devices descend from it.
- Decided
- Oct 5, 2006
- Review
- 55 days
- Class
- Class II
- Product code
- JAK
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 5 generations to K954355 (1995). 17 ancestors in all, the oldest K880965 (1988). 169 later devices descend from it, 2 citing it directly. 1 of the 187 devices in this family, counting this one, has a Class I recall.
- Root · 5 generations backK954355 Advantage Windows 3D with Navigator OptionGeneral Electric Co. · 1995
- 4 generations backK974715 Advantage 3D XRGE Medical Systems · 1998
- 3 generations backK984634 3D-AngioSiemens Medical Corp. · 1999
- 2 generations backK011447 IN Space 3DSiemens Medical Solutions USA, Inc. · 2001
- 1 generation backK043469 Syngo Inspace 4DSiemens AG Medical Solutions · 2005
- This deviceK062351 Syngo Dual EnergySiemens Medical Solutions USA, Inc. · 2006
- Descendant · cites it directly · 168 of its ownK073003 Syngo Dual Energy with Extended FunctionallySiemens Medi Cal Solutions, Inc. · 2008
- Descendant · 2 generations on · 117 of its ownK083524 Syngo Dual Energy with Extended FunationallySiemens Medical Solutions USA, Inc. · 2009
- Descendant · 3 generations on · 99 of its ownK112020 Syngo.CT Vascular AnalysisSiemens Medi Cal Solutions, Inc. · 2011
- Descendant · 4 generations on · 63 of its ownK123920 Syngo.ViaSiemens AG Medical Solutions · 2013
- Descendant · 2 generations on · 54 of its ownK093621 Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc. · 2010
Showing 5 of 169 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K250443 MAGNETOM Avanto Fit; MAGNETOM Skyra Fit…7 generations on · 2025
Most influential descendants
Showing 5 of 169 · See all- K073003Syngo Dual Energy with Extended FunctionallySiemens Medi Cal Solutions, Inc. · 2008 · cites it directly168descendants
- K083524Syngo Dual Energy with Extended FunationallySiemens Medical Solutions USA, Inc. · 2009 · 2 generations on117descendants
- K112020Syngo.CT Vascular AnalysisSiemens Medi Cal Solutions, Inc. · 2011 · 3 generations on99descendants
- K123920Syngo.ViaSiemens AG Medical Solutions · 2013 · 4 generations on63descendants
- K093621Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc. · 2010 · 2 generations on54descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K954355 | Advantage Windows 3D with Navigator Option | General Electric Co. | 1995 | — |
| −4 | K974715 | Advantage 3D XR | GE Medical Systems | 1998 | — |
| −3 | K984634 | 3D-Angio | Siemens Medical Corp. | 1999 | — |
| −2 | K011447 | IN Space 3D | Siemens Medical Solutions USA, Inc. | 2001 | — |
| −1 | K043469 | Syngo Inspace 4D | Siemens AG Medical Solutions | 2005 | — |
| 0 (this device) | K062351 | Syngo Dual Energy | Siemens Medical Solutions USA, Inc. | 2006 | — |
| +1 | K073003 | Syngo Dual Energy with Extended Functionally | Siemens Medi Cal Solutions, Inc. | 2008 | — |
| +2 | K083524 | Syngo Dual Energy with Extended Funationally | Siemens Medical Solutions USA, Inc. | 2009 | — |
| +3 | K112020 | Syngo.CT Vascular Analysis | Siemens Medi Cal Solutions, Inc. | 2011 | — |
| +4 | K123920 | Syngo.Via | Siemens AG Medical Solutions | 2013 | — |
| +2 | K093621 | Syngo.Pet&CT Oncology | Siemens Medical Solutions USA, Inc. | 2010 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1988 | 2 | 0 |
| 1991 | 1 | 0 |
| 1998 | 3 | 0 |
| 2000 | 1 | 0 |
| 2001 | 2 | 0 |
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
| 2010 | 1 | 0 |
| 2011 | 2 | 0 |
| 2012 | 5 | 0 |
| 2013 | 3 | 0 |
| 2014 | 7 | 0 |
| 2015 | 7 | 0 |
| 2016 | 8 | 0 |
| 2017 | 7 | 0 |
| 2018 | 11 | 0 |
| 2019 | 12 | 0 |
| 2020 | 18 | 0 |
| 2021 | 7 | 0 |
| 2022 | 16 | 0 |
| 2023 | 16 | 0 |
| 2024 | 15 | 0 |
| 2025 | 17 | 1 |
| 2026 | 15 | 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.
1 device in this family has a Class I recall. 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? (4)
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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K040970 | LeonardoSummary page 2…Manufacturer Product 51(k) Clearance date I. Sicmens Leonardo K040970 07/08/04 (Si n. I) Fsed I :,io… | 2004 |
| * | K043469 | Syngo Inspace 4DSummary page 2…(Si n. I) Fsed I :,ioI 31)) 2. Siemens InSpace 4D K043469 0 2 /00 3. Siemens Body Perfusion K050867 04/14/05… | 2005 |
| * | K050867 | Syngo Body Perfusion-CTSummary page 2…2. Siemens InSpace 4D K043469 0 2 /00 3. Siemens Body Perfusion K050867 04/14/05 4. Siemens SOMATOM DR I K837107 03/09/83… | 2005 |
| Kept off the family tree | K830710 | FDA’s K830710 is Argyle Silicone Salem Sump Tube Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree | 1983 |
What descends from it? (169)
See all 1692 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K250443MAGNETOM Avanto Fit; MAGNETOM Skyra Fit; MAGNETOM Sola Fit; MAGNETOM Viato.MobileSiemens Healthcare GmbH · 2025 · 7 generations on · ◆ in the 2025 descendants bar of FIG. 12 Class I recalls
What does this lineage say?
- The line of descent spans 11 years and passes through 5 companies; a new generation was cleared every 2.4 years on median.
- 3 of the 17 ancestors have a recall of any class.
- Of its descendants, K073003 (Siemens Medi Cal Solutions, Inc., 2008) has gone furthest, with 168 descendants of its own.
- 10 other devices also cite its predicate K040970.
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.
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?
Syngo Dual Energy is designed to operate with Siemens Dual Source CT scanners. CT images taken at the same time, using two different kV levels, of the same anatomical region of a patient are used. Depending on the region of interest, contrast agents may be used. The differences im the energy dependence of the attenuation coefficient of the different materials provide information about the chemical composition of body materials.
The images are combined to visualize and analyze information about anatomical and pathological structures
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062351 · printed Nov 6, 2026
Cite this page
510(k) Report. “K062351: Syngo Dual Energy.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062351
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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