# K153056: Hermes Medical Imaging Suite v5.6

- Pathway: 510(k) (Traditional)
- Applicant: Hermes Medical Solutions AB
- Decided: Jun 1, 2016 after 224 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K010641 (2001). 26 ancestors in all.
10 later devices descend from it; 3 cite it directly.
0 of 37 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142631: Hermes Medical Imaging Suite v5.5, Hermes Medical Solutions AB (2014) Summary page 4.
- K131233: Hermes Medical Imaging Suite V5.3, Hermes Medical Solutions AB (2013) Summary page 4.
- K130884: Xeleris 3.1 Processing and Review Workstation, Ge Medical Systems F.I. Haifa (2013) Summary page 4.

## Most influential descendants
- K163394: Hybrid3D (2017), 6 descendants of its own
- K171719: Hybrid3D (2017), 5 descendants of its own
- K181468: Hybrid3D (2018), 4 descendants of its own
- K171681: Hermes Medical Imaging Suite v5.7 (2017), 2 descendants of its own
- K241364: Hybrid Viewer (00859873006189) (2024), 1 descendant of its own

## Indications for use
HERMES Medical Imaging Suite that provides software applications used to process, display, analyze and manage nuclear medicine and other medical imaging data transferred from other workstation or acquistion stations.

Source page: https://510kreport.com/device/K153056
Methodology: https://510kreport.com/methodology