# K121278: Hermes Medical Imaging Suite V5.2

- Pathway: 510(k) (Special)
- Applicant: Hermes Medical Solutions AB
- Decided: Dec 18, 2012 after 232 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: 2 generations back to K002782 (2000). 2 ancestors in all.
18 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002782: Hermes HD AQ Acquisition Station and Hermes Workstation, Nuclear Diagnostics AB (2000) Summary page 1.
- K021656: Hermes Hdaq Acquisition Station and Hermes Workstation, Ver. 3.4, Nuclear Diagnostics (2002) Summary page 1.

## Most influential descendants
- K131233: Hermes Medical Imaging Suite V5.3 (2013), 16 descendants of its own
- K140269: Hermes Medical Imaging Suite V5.4 (2014), 15 descendants of its own
- K142631: Hermes Medical Imaging Suite v5.5 (2014), 11 descendants of its own
- K153056: Hermes Medical Imaging Suite v5.6 (2016), 10 descendants of its own
- K163394: Hybrid3D (2017), 6 descendants 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 acquisition stations.

Source page: https://510kreport.com/device/K121278
Methodology: https://510kreport.com/methodology