510(k) Report

510(k) · Cleared

Cleared

Deep Learning Image Reconstruction

K193170510(k) SpecialCleared Dec 13, 201928-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

Ge Healthcare Japan Corporation · JAK System, X-Ray, Tomography, Computed

Cleared on Dec 13, 2019 as substantially equivalent to K183202 (Ge Medical Systems, LLC, 2019) after a 28-day review. Its family tree reaches back 9 generations to 2001. 1 later device descends from it.

Decided
Dec 13, 2019
Review
28 days
Class
Class II
Product code
JAK
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K013561 (2001). 14 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 9 generations backK013561 Lightspeed 4.0 CT Scanner SystemGE Medical Systems · 2001 · Recalled
  2. 5 generations between
  3. 3 generations backK133705 Revolution CTGe Medical Systems, LLC · 2014 · Recalled
  4. 2 generations backK163213 Revolution CTGe Medical Systems, LLC · 2016 · Recalled
  5. 1 generation backK183202 Deep Learning Image ReconstructionGe Medical Systems, LLC · 2019
  6. This deviceK193170 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2019
  7. Descendant · cites it directly · 0 of its ownK212067 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2021
Show all 9 generations
  1. Root · 9 generations backK013561 Lightspeed 4.0 CT Scanner SystemGE Medical Systems · 2001 · Recalled
  2. 8 generations backK030420 Lightspeed 5.0 Computed Tomography SystemGE Medical Systems · 2003 · Recalled
  3. 7 generations backK040372 Lightspeed 7.0 CT Scanner SystemGe Medical Systems, LLC · 2004 · Recalled
  4. 6 generations backK061817 Lightspeed 7.1 CT Scanner SystemGe Medical Systems, LLC · 2006 · Recalled
  5. 5 generations backK081105 GE Lightspeed CT750 HD (Lightspeed 8.0)GE Healthcare · 2008 · Recalled
  6. 4 generations backK120833 Discovery CT750 HDGe Medical Systems, LLC · 2012 · Recalled
  7. 3 generations backK133705 Revolution CTGe Medical Systems, LLC · 2014 · Recalled
  8. 2 generations backK163213 Revolution CTGe Medical Systems, LLC · 2016 · Recalled
  9. 1 generation backK183202 Deep Learning Image ReconstructionGe Medical Systems, LLC · 2019
  10. This deviceK193170 Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2019

Most influential descendants

Showing 1 of 1 · See all
  • K212067Deep Learning Image ReconstructionGe Healthcare Japan Corporation · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K013561Lightspeed 4.0 CT Scanner SystemGE Medical Systems20015
−8K030420Lightspeed 5.0 Computed Tomography SystemGE Medical Systems20034
−7K040372Lightspeed 7.0 CT Scanner SystemGe Medical Systems, LLC20045
−6K061817Lightspeed 7.1 CT Scanner SystemGe Medical Systems, LLC20061
−5K081105GE Lightspeed CT750 HD (Lightspeed 8.0)GE Healthcare20085
−4K120833Discovery CT750 HDGe Medical Systems, LLC20121
−3K133705Revolution CTGe Medical Systems, LLC201414
−2K163213Revolution CTGe Medical Systems, LLC201616
−1K183202Deep Learning Image ReconstructionGe Medical Systems, LLC2019—
0 (this device)K193170Deep Learning Image ReconstructionGe Healthcare Japan Corporation2019—
+1K212067Deep Learning Image ReconstructionGe Healthcare Japan Corporation2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200610
200810
201120
201410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
FIG. 1 — Lineage of K193170, 2001–2021Source: 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
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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
*K183202Deep Learning Image Reconstruction
Summary page 4
…mation Device Name: Deep Learning Image Reconstruction Manufacturer: GE Medical System SCS (d.b.a GE Healthcare) 510(k) Number: K183202 cleared on April 12, 2019 Regulation Number/ 21 CFR 892.1750 Computed tomography x-ray system / JAK Product Code: Re…
Ge Medical Systems, LLC2019—
†K133640ASIR-VGe Medical Systems, LLC2014—

Also cleared against K183202: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K212067Deep Learning Image ReconstructionGe Healthcare Japan Corporation20210

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 18 years and passes through 4 companies; a new generation was cleared every 1.8 years on median.
  • 11 of the 14 ancestors have a recall of any class.
  • Of its descendants, K212067 (Ge Healthcare Japan Corporation, 2021) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K183202.

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?

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 read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K193170: Deep Learning Image Reconstruction.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K193170

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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