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 Feb 10, 2026 as substantially equivalent to K242300 (Siemens Medical Solutions USA, Inc., 2024) and 1 other predicate after a 57-day review. Its family tree reaches back 23 generations to 1991.
- Decided
- Feb 10, 2026
- Review
- 57 days
- Class
- Class II
- Product code
- QIH
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 23 generations to K913770 (1991). 154 ancestors in all, the oldest K871859 (1987). No later device cites it as a predicate yet.
- Root · 23 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- 19 generations between
- 3 generations backK232000 syngo.via MI Workflows; Scenium; syngo MBFSiemens Medical Solutions USA, Inc. · 2023
- 2 generations backK242275 syngo.via MI Workflows; Scenium; syngo MBFSiemens Medical Solutions USA, Inc. · 2024
- 1 generation backK251528 syngo.via MI Workflows; Scenium; syngo MBFSiemens Medical Solutions USA, Inc. · 2025
- This deviceK254016 MI View&GOSiemens Medical Solutions USA, Inc. · 2026
Show all 23 generations
- Root · 23 generations backK913770 Advantage V.S. CT/MR Rad Diagnostic WorkstationGeneral Electric Co. · 1991
- 22 generations backK963345 Advantage Windows Tissue Volume OptionGE Medical Systems · 1996
- 21 generations backK013381 Advanced Lung Analysis-1General Electric Co. · 2001
- 20 generations backK022013 Lungcare CT Software PackageSiemens Medical Solutions USA, Inc. · 2002
- 19 generations backK033374 Lungcare CT Software Package with Extended FunctionalitySiemens AG Medical Solutions · 2003
- 18 generations backK041484 UndecidedSiemens Medical Solutions USA, Inc. · 2004
- 17 generations backK053301 Cedara I-Response Cedara Pet/CTCedara Software Corp. · 2006
- 16 generations backK071950 Syngo TruedSiemens Medical Solutions USA, Inc. · 2007
- 15 generations backK091373 Syngo TruedSiemens Medical Solutions USA, Inc. · 2009
- 14 generations backK093621 Syngo.Pet&CT OncologySiemens Medical Solutions USA, Inc. · 2010
- 13 generations backK113029 Syngo Via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2011
- 12 generations backK123577 Syngo.Via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2013
- 11 generations backK133644 Syngo.Via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2014
- 10 generations backK151192 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2015
- 9 generations backK160426 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2016
- 8 generations backK163421 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2017
- 7 generations backK173897 syngo.via MI WorkflowsSiemens Medical Solutions USA, Inc. · 2018
- 6 generations backK191309 syngo.via MI Workflows VB40A, SceniumSiemens Medical Soultions USA, Inc. · 2019
- 5 generations backK201195 syngo.via MI Workflows, syngo MBFSiemens Medical Solutions USA, Inc. · 2020
- 4 generations backK211459 syngo.via MI WorkFlows, Scenium, syngo MBFSiemens Medical Solutions USA, Inc. · 2021
- 3 generations backK232000 syngo.via MI Workflows; Scenium; syngo MBFSiemens Medical Solutions USA, Inc. · 2023
- 2 generations backK242275 syngo.via MI Workflows; Scenium; syngo MBFSiemens Medical Solutions USA, Inc. · 2024
- 1 generation backK251528 syngo.via MI Workflows; Scenium; syngo MBFSiemens Medical Solutions USA, Inc. · 2025
- This deviceK254016 MI View&GOSiemens Medical Solutions USA, Inc. · 2026
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −23 | K913770 | Advantage V.S. CT/MR Rad Diagnostic Workstation | General Electric Co. | 1991 | — |
| −22 | K963345 | Advantage Windows Tissue Volume Option | GE Medical Systems | 1996 | — |
| −21 | K013381 | Advanced Lung Analysis-1 | General Electric Co. | 2001 | — |
| −20 | K022013 | Lungcare CT Software Package | Siemens Medical Solutions USA, Inc. | 2002 | — |
| −19 | K033374 | Lungcare CT Software Package with Extended Functionality | Siemens AG Medical Solutions | 2003 | — |
| −18 | K041484 | Undecided | Siemens Medical Solutions USA, Inc. | 2004 | — |
| −17 | K053301 | Cedara I-Response Cedara Pet/CT | Cedara Software Corp. | 2006 | — |
| −16 | K071950 | Syngo Trued | Siemens Medical Solutions USA, Inc. | 2007 | — |
| −15 | K091373 | Syngo Trued | Siemens Medical Solutions USA, Inc. | 2009 | — |
| −14 | K093621 | Syngo.Pet&CT Oncology | Siemens Medical Solutions USA, Inc. | 2010 | — |
| −13 | K113029 | Syngo Via MI Workflows | Siemens Medical Solutions USA, Inc. | 2011 | — |
| −12 | K123577 | Syngo.Via MI Workflows | Siemens Medical Solutions USA, Inc. | 2013 | — |
| −11 | K133644 | Syngo.Via MI Workflows | Siemens Medical Solutions USA, Inc. | 2014 | — |
| −10 | K151192 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2015 | — |
| −9 | K160426 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2016 | — |
| −8 | K163421 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2017 | — |
| −7 | K173897 | syngo.via MI Workflows | Siemens Medical Solutions USA, Inc. | 2018 | — |
| −6 | K191309 | syngo.via MI Workflows VB40A, Scenium | Siemens Medical Soultions USA, Inc. | 2019 | — |
| −5 | K201195 | syngo.via MI Workflows, syngo MBF | Siemens Medical Solutions USA, Inc. | 2020 | — |
| −4 | K211459 | syngo.via MI WorkFlows, Scenium, syngo MBF | Siemens Medical Solutions USA, Inc. | 2021 | — |
| −3 | K232000 | syngo.via MI Workflows; Scenium; syngo MBF | Siemens Medical Solutions USA, Inc. | 2023 | — |
| −2 | K242275 | syngo.via MI Workflows; Scenium; syngo MBF | Siemens Medical Solutions USA, Inc. | 2024 | — |
| −1 | K251528 | syngo.via MI Workflows; Scenium; syngo MBF | Siemens Medical Solutions USA, Inc. | 2025 | — |
| 0 (this device) | 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 | 4 | 0 |
| 2009 | 2 | 0 |
| 2011 | 1 | 0 |
| 2020 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 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? (2)
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 |
|---|---|---|---|
| * | K242300 | MI View&GOSummary page 5…evice Class: Class II Product Code: QIH 3. Predicate Devices Primary Predicate Device: Product Trade Name: MI View&GO 510(k) Number: K242300 Clearance Date: 08/02/2024 Common Name: Medical image management and processing system Classification Name:… | 2024 |
| * | K251528 | syngo.via MI Workflows; Scenium; syngo MBFSummary page 6…1 Predicate / Reference Device Trade Name: syngo.via MI Workflows 510(k) Number: K251528 Clearance Date: 05/19/2025 Common Name: Medical image management and processing system Classification Name:… | 2025 |
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 35 years and passes through 6 companies; a new generation was cleared every 1.3 years on median.
- 33 of the 154 ancestors have a recall of any class.
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. 2026, 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 as stated in the FDA summary.
https://510kreport.com/device/K254016 · printed Nov 5, 2026
Cite this page
510(k) Report. “K254016: MI View&GO.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K254016
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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