510(k) · Cleared
ClearedHermes Medical Imaging Suite V5.3
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hermes Medical Solutions AB · KPS System, Tomography, Computed, Emission
Cleared on Jul 16, 2013 as substantially equivalent to K121278 (Hermes Medical Solutions AB, 2012) and 3 other predicates after a 76-day review. Its family tree reaches back 3 generations to 2000. 16 later devices descend from it.
- Decided
- Jul 16, 2013
- Review
- 76 days
- Class
- Class II
- Product code
- KPS
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 3 generations to K000395 (2000). 6 ancestors in all. 16 later devices descend from it, 3 citing it directly.
- Root · 3 generations backK000395 Einstein Processing and Review WorkstationGe Medical Systems F.I. Haifa · 2000
- 2 generations backK024137 Jupiter Processing and Review WorkstationGe Medical Systems, Inc. · 2003 · Recalled
- 1 generation backK051673 Xeleris 2 Processing and Review WorkstationGE Medical Systems · 2005 · Recalled
- This deviceK131233 Hermes Medical Imaging Suite V5.3Hermes Medical Solutions AB · 2013
- Descendant · cites it directly · 15 of its ownK140269 Hermes Medical Imaging Suite V5.4Hermes Medical Solutions AB · 2014
- Descendant · cites it directly · 11 of its ownK142631 Hermes Medical Imaging Suite v5.5Hermes Medical Solutions AB · 2014
- Descendant · cites it directly · 10 of its ownK153056 Hermes Medical Imaging Suite v5.6Hermes Medical Solutions AB · 2016
- Descendant · 2 generations on · 6 of its ownK163394 Hybrid3DHermes Medical Solutions AB · 2017
- Descendant · 2 generations on · 5 of its ownK171719 Hybrid3DHermes Medical Solutions AB · 2017
Showing 5 of 16 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 16 · See all- K140269Hermes Medical Imaging Suite V5.4Hermes Medical Solutions AB · 2014 · cites it directly15descendants
- K142631Hermes Medical Imaging Suite v5.5Hermes Medical Solutions AB · 2014 · cites it directly11descendants
- K153056Hermes Medical Imaging Suite v5.6Hermes Medical Solutions AB · 2016 · cites it directly10descendants
- K163394Hybrid3DHermes Medical Solutions AB · 2017 · 2 generations on6descendants
- K171719Hybrid3DHermes Medical Solutions AB · 2017 · 2 generations on5descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K000395 | Einstein Processing and Review Workstation | Ge Medical Systems F.I. Haifa | 2000 | — |
| −2 | K024137 | Jupiter Processing and Review Workstation | Ge Medical Systems, Inc. | 2003 | 2 |
| −1 | K051673 | Xeleris 2 Processing and Review Workstation | GE Medical Systems | 2005 | 3 |
| 0 (this device) | K131233 | Hermes Medical Imaging Suite V5.3 | Hermes Medical Solutions AB | 2013 | — |
| +1 | K140269 | Hermes Medical Imaging Suite V5.4 | Hermes Medical Solutions AB | 2014 | — |
| +1 | K142631 | Hermes Medical Imaging Suite v5.5 | Hermes Medical Solutions AB | 2014 | — |
| +1 | K153056 | Hermes Medical Imaging Suite v5.6 | Hermes Medical Solutions AB | 2016 | — |
| +2 | K163394 | Hybrid3D | Hermes Medical Solutions AB | 2017 | — |
| +2 | K171719 | Hybrid3D | Hermes Medical Solutions AB | 2017 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 1 | 0 |
| 2002 | 1 | 0 |
| 2012 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 2 | 0 |
| 2016 | 2 | 0 |
| 2017 | 3 | 0 |
| 2018 | 1 | 0 |
| 2020 | 3 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2024 | 1 | 0 |
| 2025 | 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 KPS? 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 KPS device
- #1 K253564 uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI…score 18.6 · 17 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K121278 | Hermes Medical Imaging Suite V5.2Summary page 1…CFR892.1200 0. Legally marketed device (predicate device): Following legally marketed device has been used for comparison. * HERMES Medical Imaging Workstation (K121278) * HERMES HDAQ Acquisition Station and Hermes Workstation (K021656) * HERMES HDAO Acquisition Station and Hermes Work… | 2012 |
| * | K021656 | Hermes Hdaq Acquisition Station and Hermes Workstation, Ver. 3.4Summary page 1…gally marketed device has been used for comparison. * HERMES Medical Imaging Workstation (K121278) * HERMES HDAQ Acquisition Station and Hermes Workstation (K021656) * HERMES HDAO Acquisition Station and Hermes Workstation (K002782) * Xeleris 2 processing and review workstation (K0… | 2002 |
| * | K002782 | Hermes HD AQ Acquisition Station and Hermes WorkstationSummary page 1…al Imaging Workstation (K121278) * HERMES HDAQ Acquisition Station and Hermes Workstation (K021656) * HERMES HDAO Acquisition Station and Hermes Workstation (K002782) * Xeleris 2 processing and review workstation (K051673) E. Description of the device that is subject of this premarket no… | 2000 |
| * | K051673 | Xeleris 2 Processing and Review WorkstationSummary page 1…on Station and Hermes Workstation (K021656) * HERMES HDAO Acquisition Station and Hermes Workstation (K002782) * Xeleris 2 processing and review workstation (K051673) E. Description of the device that is subject of this premarket notification: The base product design of Hermes Medical Imaging… | 2005 |
What descends from it? (16)
See all 163 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 13 years and passes through 4 companies; a new generation was cleared every 2.7 years on median.
- 2 of the 6 ancestors have a recall of any class.
- Of its descendants, K140269 (Hermes Medical Solutions AB, 2014) has gone furthest, with 15 descendants of its own.
- 1 other device also cites its predicate K121278.
How does its category compare?
All KPS devicesKPS System, Tomography, Computed, Emission: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · KPS
12in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KPS
65in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KPS
16in 2025
Class I (17 since 2007) Class II/III not classified
Adverse event reports per year · KPS
36in 2025
MAUDE reports naming product code KPS, 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 | 8 | 38 | 22 | 38 |
| 2008 | 17 | 25 | 16 | 11 |
| 2009 | 9 | 42 | 14 | 15 |
| 2010 | 3 | 91 | 4 | 44 |
| 2011 | 7 | 28 | 34 | 56 |
| 2012 | 6 | 94 | 13 | 34 |
| 2013 | 11 | 84 | 13 | 240 |
| 2014 | 11 | 92 | 18 | 33 |
| 2015 | 3 | 112 | 5 | 24 |
| 2016 | 11 | 65 | 16 | 10 |
| 2017 | 11 | 104 | 11 | 31 |
| 2018 | 13 | 59 | 12 (3) | 26 |
| 2019 | 3 | 60 | 5 (5) | 105 |
| 2020 | 12 | 72 | 8 | 22 |
| 2021 | 15 | 66 | 4 | 10 |
| 2022 | 5 | 60 | 8 (6) | 15 |
| 2023 | 12 | 63 | 6 (3) | 22 |
| 2024 | 11 | 59 | 15 | 23 |
| 2025 | 12 | 65 | 16 | 36 |
| 2026 | 6 | 67 | 6 | — |
What is it indicated for?
HERMES Medical Imaging suite that provides software application used to process, display, analyze and manage nuclear medicine and other medical imaging data transferred from other workstation or acquisition stations.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K131233 · printed Nov 6, 2026
Cite this page
510(k) Report. “K131233: Hermes Medical Imaging Suite V5.3.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K131233
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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