510(k) · Cleared
ClearedMI View&GO
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Siemens Medical Solutions USA, Inc. · QIH Automated Radiological Image Processing Software
Cleared on Aug 19, 2022 as substantially equivalent to K201202 (Siemens Medical Solutions USA, Inc., 2020) after a 29-day review. Its family tree reaches back 19 generations to 1991. 2 later devices descend from it.
- Decided
- Aug 19, 2022
- Review
- 29 days
- Class
- Class II
- Product code
- QIH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 19 generations to K913770 (1991). 144 ancestors in all, the oldest K871859 (1987). 2 later devices descend from it, 1 citing it directly.
- Root · 19 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- 15 generations between
- 3 generations backK173897 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2018
- 2 generations backK191309 syngo.via MI Workflows VB40A, SceniumSiemens Medical Soultions USA, Inc. · 2019
- 1 generation backK201202 MI View&GOSiemens Medical Solutions USA, Inc. · 2020
- This deviceK222172 MI View&GOSiemens Medical Solutions USA, Inc. · 2022
- Descendant · cites it directly · 1 of its ownK242300 MI View&GOSiemens Medical Solutions USA, Inc. · 2024
- Descendant · 2 generations on · 0 of its ownK254016 MI View&GOSiemens Medical Solutions USA, Inc. · 2026
Show all 19 generations
- Root · 19 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- 18 generations backK963345 Advantage Windows Tissue Volume OptionGE Medical Systems · 1996
- 17 generations backK013381 Advanced Lung Analysis-1General Electric Co. · 2001
- 16 generations backK022013 Lungcare CT Software PackageSiemens Medical Solutions USA, Inc. · 2002
- 15 generations backK033374 Lungcare CT Software Package with Extended FunctionalitySiemens AG Medical Solutions · 2003
- 14 generations backK041484 UndecidedSiemens Medical Solutions USA, Inc. · 2004
- 13 generations backK053301 Cedara I-Response Cedara Pet/CTCedara Software Corp. · 2006
- 12 generations backK071950 Syngo TruedSiemens Medical Solutions USA, Inc. · 2007
- 11 generations backK091373 Syngo TruedSiemens Medical Solutions USA, Inc. · 2009
- 10 generations backK093621 Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc. · 2010
- 9 generations backK113029 Syngo Via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2011
- 8 generations backK123577 Syngo.Via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2013
- 7 generations backK133644 Syngo.Via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2014
- 6 generations backK151192 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2015
- 5 generations backK160426 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2016
- 4 generations backK163421 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2017
- 3 generations backK173897 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2018
- 2 generations backK191309 syngo.via MI Workflows VB40A, SceniumSiemens Medical Soultions USA, Inc. · 2019
- 1 generation backK201202 MI View&GOSiemens Medical Solutions USA, Inc. · 2020
- This deviceK222172 MI View&GOSiemens Medical Solutions USA, Inc. · 2022
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −19 | K913770 | Advantage V.S. CT/MR Rad Diagnostic Workstation | General Electric Co. | 1991 | — |
| −18 | K963345 | Advantage Windows Tissue Volume Option | GE Medical Systems | 1996 | — |
| −17 | K013381 | Advanced Lung Analysis-1 | General Electric Co. | 2001 | — |
| −16 | K022013 | Lungcare CT Software Package | Siemens Medical Solutions USA, Inc. | 2002 | — |
| −15 | K033374 | Lungcare CT Software Package with Extended Functionality | Siemens AG Medical Solutions | 2003 | — |
| −14 | K041484 | Undecided | Siemens Medical Solutions USA, Inc. | 2004 | — |
| −13 | K053301 | Cedara I-Response Cedara Pet/CT | Cedara Software Corp. | 2006 | — |
| −12 | K071950 | Syngo Trued | Siemens Medical Solutions USA, Inc. | 2007 | — |
| −11 | K091373 | Syngo Trued | Siemens Medical Solutions USA, Inc. | 2009 | — |
| −10 | K093621 | Syngo.Pet&CT Oncology | Siemens Medical Solutions USA, Inc. | 2010 | — |
| −9 | K113029 | Syngo Via MI Workflows | Siemens Medical Solutions USA, Inc. | 2011 | — |
| −8 | K123577 | Syngo.Via MI Workflows | Siemens Medical Solutions USA, Inc. | 2013 | — |
| −7 | K133644 | Syngo.Via MI Workflows | Siemens Medical Solutions USA, Inc. | 2014 | — |
| −6 | K151192 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2015 | — |
| −5 | K160426 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2016 | — |
| −4 | K163421 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2017 | — |
| −3 | K173897 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2018 | — |
| −2 | K191309 | syngo.via MI Workflows VB40A, Scenium | Siemens Medical Soultions USA, Inc. | 2019 | — |
| −1 | K201202 | MI View&GO | Siemens Medical Solutions USA, Inc. | 2020 | — |
| 0 (this device) | K222172 | MI View&GO | Siemens Medical Solutions USA, Inc. | 2022 | — |
| +1 | K242300 | MI View&GO | Siemens Medical Solutions USA, Inc. | 2024 | — |
| +2 | K254016 | MI View&GO | Siemens Medical Solutions USA, Inc. | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1988 | 2 | 0 |
| 1989 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 5 | 0 |
| 1992 | 2 | 0 |
| 1993 | 2 | 0 |
| 1994 | 3 | 0 |
| 1995 | 4 | 0 |
| 1996 | 7 | 0 |
| 1997 | 6 | 0 |
| 1998 | 11 | 0 |
| 1999 | 5 | 0 |
| 2000 | 8 | 0 |
| 2001 | 13 | 0 |
| 2002 | 11 | 0 |
| 2003 | 5 | 0 |
| 2004 | 12 | 0 |
| 2005 | 9 | 0 |
| 2006 | 7 | 0 |
| 2007 | 6 | 0 |
| 2008 | 3 | 0 |
| 2009 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2024 | 1 | 0 |
| 2026 | 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 QIH? 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 QIH device
- #1 K213998 cvi42 Auto Imaging Software Applicationscore 23.5 · 7 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 |
|---|---|---|---|
| * | K201202 | MI View&GOSummary page 5…ology Device Class: Class II Manufacturer: Siemens Medical Solutions USA, inc. 510(k) Number: K201202 (June 2020) Reference Predicate Device Device Proprietary Name: syngo.via MI Workflows VB60A Common Name:… | 2020 |
| † | K211459 | syngo.via MI WorkFlows, Scenium, syngo MBF | 2021 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K242300 | MI View&GO | 2024 | 1 |
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 31 years and passes through 6 companies; a new generation was cleared every 1.3 years on median.
- 33 of the 144 ancestors have a recall of any class.
- Of its descendants, K242300 (Siemens Medical Solutions USA, Inc., 2024) has gone furthest, with 1 descendant of its own.
- 1 other device also cites its predicate K201202.
How does its category compare?
All QIH devicesQIH Automated Radiological Image Processing Software: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · QIH
94in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · QIH
150in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QIH
1so far in 2026, the most since 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · QIH
4in 2025
MAUDE reports naming product code QIH, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 2 | — | 0 | 0 |
| 2020 | 11 | 145 | 0 | 0 |
| 2021 | 19 | 125 | 0 | 0 |
| 2022 | 25 | 134 | 0 | 0 |
| 2023 | 45 | 151 | 0 | 0 |
| 2024 | 64 | 141 | 0 | 2 |
| 2025 | 94 | 150 | 0 | 4 |
| 2026 | 78 | 130 | 1 | — |
What is it indicated for?
MI View& GO is a medical diagnostic application for viewing, manipulation, quantification, analysis and comparison of medical images with one or more time-points. MI View&GO supports functional data, such as positron emission tomography (PET) or nuclear medicine (NM), as well as anatomical datasets, such as computed tomography (CT) or magnetic resonance (MR).
MI View& GO is intended to be utilized by appropriately trained health care professionals to aid in the management of diseases associated with oncology, cardiology, neurology, and organ function. The images and results produced by MI View&GO can also be used by the physician to aid in radiotherapy treatment planning.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K222172 · printed Nov 6, 2026
Cite this page
510(k) Report. “K222172: MI View&GO.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K222172
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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