# K002782: Hermes HD AQ Acquisition Station and Hermes Workstation

- Pathway: 510(k) (Traditional)
- Applicant: Nuclear Diagnostics AB
- Decided: Dec 5, 2000 after 90 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
97 later devices descend from it; 5 cite it directly.
0 of 98 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021656: Hermes Hdaq Acquisition Station and Hermes Workstation, Ver. 3.4 (2002), 93 descendants of its own
- K121074: Scenium 2.0 (2012), 90 descendants of its own
- K123528: Scenium (2012), 79 descendants of its own
- K130884: Xeleris 3.1 Processing and Review Workstation (2013), 77 descendants of its own
- K153355: Xeleris 4.0 Processing and Review Workstation (2016), 60 descendants of its own

Source page: https://510kreport.com/device/K002782
Methodology: https://510kreport.com/methodology