# K003222: Modification to Hermes Operating Room Control Center

- Pathway: 510(k) (Special)
- Applicant: Computer Motion, Inc.
- Decided: Nov 3, 2000 after 18 days
- Product code: GCI (Laryngoscope, Endoscope)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 2 cite it directly.
0 of 12 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
- K023095: Hermes Operating Room Control Center (2002), 9 descendants of its own
- K024294: Modification to Hermes Operating Room Control Center (2003), 8 descendants of its own
- K030240: Modification to Hermes Operating Room Control Center (2003), 7 descendants of its own
- K052740: Nurse's Assistant 1.7 O.R. Control System (2005), 2 descendants of its own
- K060717: Nurse Assistant 1.7 O.R. Control System (2006), 1 descendant of its own

Source page: https://510kreport.com/device/K003222
Methodology: https://510kreport.com/methodology