510(k) Report

510(k) · Cleared

Cleared

Aquilion ONE (TSX-306A/3) V10.0

K192188510(k) SpecialCleared Sep 6, 201924-day reviewClass II21 CFR 892.1750

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Canon Medical Systems Corporation · JAK System, X-Ray, Tomography, Computed

Cleared on Sep 6, 2019 as substantially equivalent to K183046 (Canon Medical Systems Corporation, 2019) after a 24-day review. Its family tree reaches back 9 generations to 2012. 9 later devices descend from it.

Decided
Sep 6, 2019
Review
24 days
Class
Class II
Product code
JAK
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K113466 (2012). 10 ancestors in all. 9 later devices descend from it, 1 citing it directly.

  1. Root · 9 generations backK113466 Aquilion OneToshiba Medical Systems Coporation, Japan · 2012 · Recalled
  2. 5 generations between
  3. 3 generations backK161009 Aquilion ONE Vision with FIRST 2.0 (CCRS-001B) V7.4Toshibamedical Systems Corporation · 2016
  4. 2 generations backK170177 Aquilion ONE (TSX-305A/3) V8.3 with FIRST 2.1Toshibamedical Systems Corporation · 2017 · Recalled
  5. 1 generation backK183046 Aquilion ONE (TSX-305A/6) V8.9 with AiCECanon Medical Systems Corporation · 2019
  6. This deviceK192188 Aquilion ONE (TSX-306A/3) V10.0Canon Medical Systems Corporation · 2019
  7. Descendant · cites it directly · 8 of its ownK192828 Aquilion ONE (TSX-306A/3) V10.0 with Spectral Imaging SystemCanon Medical Systems Corporation · 2020
  8. Descendant · 2 generations on · 7 of its ownK203225 Aquilion ONE (TSX-306A/3) V10.4 with Spectral Imaging SystemCanon Medical Systems Corporation · 2021
  9. Descendant · 3 generations on · 6 of its ownK213504 Aquilion ONE (TSX-306A/3) V10.12 with Spectral Imaging System…Canon Medical Systems Corporation · 2022
  10. Descendant · 4 generations on · 3 of its ownK232835 Aquilion ONE (TSX-308A/3) V1.4 with PIQE Reconstruction SystemCanon Medical Systems Corporation · 2024
  11. Descendant · 5 generations on · 2 of its ownK242403 Aquilion ONE (TSX-308A/3) V1.5Canon Medical Systems Corporation · 2024
Show all 9 generations
  1. Root · 9 generations backK113466 Aquilion OneToshiba Medical Systems Coporation, Japan · 2012 · Recalled
  2. 8 generations backK122109 Aquilion One Vision, V4.90Toshiba America Medical Systems, In.C · 2012 · Recalled
  3. 7 generations backK132222 Aquilion One Vision, V6.0Toshibamedical Systems Corporation · 2013 · Recalled
  4. 6 generations backK133497 Aquilion One VisionToshibamedical Systems Corporation · 2014
  5. 5 generations backK142465 Aquilion ONE Vision, v7.0Toshibamedical Systems Corporation · 2015 · Recalled
  6. 4 generations backK151673 Aquilion ONE Vision with FIRST 1.0 (CCRS-001A)Toshibamedical Systems Corporation · 2015 · Recalled
  7. 3 generations backK161009 Aquilion ONE Vision with FIRST 2.0 (CCRS-001B) V7.4Toshibamedical Systems Corporation · 2016
  8. 2 generations backK170177 Aquilion ONE (TSX-305A/3) V8.3 with FIRST 2.1Toshibamedical Systems Corporation · 2017 · Recalled
  9. 1 generation backK183046 Aquilion ONE (TSX-305A/6) V8.9 with AiCECanon Medical Systems Corporation · 2019
  10. This deviceK192188 Aquilion ONE (TSX-306A/3) V10.0Canon Medical Systems Corporation · 2019

Showing 5 of 9 descendants. See all descendants

Descendants cleared per year

2020: 12021: 12022: 12023: 12024: 32025: 12026: 1
2020high 3 (2024) · low 1 (2020)2026

Most influential descendants

Showing 5 of 9 · See all
  • K192828Aquilion ONE (TSX-306A/3) V10.0 with Spectral Imaging SystemCanon Medical Systems Corporation · 2020 · cites it directly8descendants
  • K203225Aquilion ONE (TSX-306A/3) V10.4 with Spectral Imaging SystemCanon Medical Systems Corporation · 2021 · 2 generations on7descendants
  • K213504Aquilion ONE (TSX-306A/3) V10.12 with Spectral Imaging System, Vitrea Software Package…Canon Medical Systems Corporation · 2022 · 3 generations on6descendants
  • K232835Aquilion ONE (TSX-308A/3) V1.4 with PIQE Reconstruction SystemCanon Medical Systems Corporation · 2024 · 4 generations on3descendants
  • K242403Aquilion ONE (TSX-308A/3) V1.5Canon Medical Systems Corporation · 2024 · 5 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K113466Aquilion OneToshiba Medical Systems Coporation, Japan20123
−8K122109Aquilion One Vision, V4.90Toshiba America Medical Systems, In.C20121
−7K132222Aquilion One Vision, V6.0Toshibamedical Systems Corporation20132
−6K133497Aquilion One VisionToshibamedical Systems Corporation2014—
−5K142465Aquilion ONE Vision, v7.0Toshibamedical Systems Corporation20151
−4K151673Aquilion ONE Vision with FIRST 1.0 (CCRS-001A)Toshibamedical Systems Corporation20151
−3K161009Aquilion ONE Vision with FIRST 2.0 (CCRS-001B) V7.4Toshibamedical Systems Corporation2016—
−2K170177Aquilion ONE (TSX-305A/3) V8.3 with FIRST 2.1Toshibamedical Systems Corporation20171
−1K183046Aquilion ONE (TSX-305A/6) V8.9 with AiCECanon Medical Systems Corporation2019—
0 (this device)K192188Aquilion ONE (TSX-306A/3) V10.0Canon Medical Systems Corporation2019—
+1K192828Aquilion ONE (TSX-306A/3) V10.0 with Spectral Imaging SystemCanon Medical Systems Corporation2020—
+2K203225Aquilion ONE (TSX-306A/3) V10.4 with Spectral Imaging SystemCanon Medical Systems Corporation2021—
+3K213504Aquilion ONE (TSX-306A/3) V10.12 with Spectral Imaging System, Vitrea Software…Canon Medical Systems Corporation2022—
+4K232835Aquilion ONE (TSX-308A/3) V1.4 with PIQE Reconstruction SystemCanon Medical Systems Corporation2024—
+5K242403Aquilion ONE (TSX-308A/3) V1.5Canon Medical Systems Corporation2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
201610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202110
202210
202310
202430
202510
202610
FIG. 1 — Lineage of K192188, 2012–2026Source: 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 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. #1 K230223 iCAC Devicescore 23.5 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K183046Aquilion ONE (TSX-305A/6) V8.9 with AiCE
Summary page 5
…21 CFR System, X‐ray, 305A/6) V8.9 with Medical Tomography K183046 06/12/2019 892.1750 Tomography, AiCE Sys…
Canon Medical Systems Corporation2019—

What descends from it? (9)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K192828Aquilion ONE (TSX-306A/3) V10.0 with Spectral Imaging SystemCanon Medical Systems Corporation20208

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 7 years and passes through 4 companies; a new generation was cleared every 9 months on median.
  • 6 of the 10 ancestors have a recall of any class.
  • Of its descendants, K192828 (Canon Medical Systems Corporation, 2020) has gone furthest, with 8 descendants of its own.

How does its category compare?

All JAK devices

JAK System, X-Ray, Tomography, Computed: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · JAK

27in 2025

2007: 142008: 262009: 152010: 72011: 162012: 282013: 172014: 302015: 302016: 252017: 292018: 242019: 282020: 302021: 202022: 302023: 272024: 262025: 272026 (partial year): 21
2007high 30 (2014) · low 7 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JAK

141in 2025

2007: 27 days median2008: 42 days median2009: 31 days median2010: 92 days median2011: 155 days median2012: 121 days median2013: 132 days median2014: 200 days median2015: 140 days median2016: 129 days median2017: 96 days median2018: 114 days median2019: 94 days median2020: 112 days median2021: 145 days median2022: 131 days median2023: 139 days median2024: 141 days median2025: 141 days median2026 (partial year): 167 days median
2007high 200 (2014) · low 27 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · JAK

17in 2025

2007: 112008: 162009: 292010: 512011: 342012: 232013: 112014: 102015: 282016: 442017: 332018: 102019: 52020: 82021: 152022: 92023: 92024: 202025: 172026 (partial year): 23
2007high 51 (2010) · low 5 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · JAK

219in 2025

2007: 762008: 1202009: 1052010: 1192011: 2052012: 1922013: 4142014: 3082015: 4542016: 3652017: 3382018: 5432019: 2332020: 1772021: 2612022: 1992023: 3102024: 2122025: 219
2007high 543 (2018) · low 76 (2007)2025

MAUDE reports naming product code JAK, 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
200714271176
2008264216120
2009153129105
201079251119
20111615534205
20122812123192
20131713211414
20143020010308
20153014028454
20162512944365
2017299633338
20182411410543
201928945233
2020301128177
20212014515261
2022301319199
2023271399310
20242614120212
20252714117219
20262116723—

What is it indicated for?

This device is indicated to acquire and display cross-sectional volumes of the whole body, to include the head, with the capability to image whole organs in a single rotation. Whole organs include, but are not limited to brain, heart, pancreas, etc.

The Aquilion ONE has the capability to provide volume sets of the entire organ. These volume sets can be used to perform specialized studies, using indicated software/hardware, of the whole organ by a trained and qualified physician.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192188: Aquilion ONE (TSX-306A/3) V10.0.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192188

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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