# K000892: Datex-Ohmeda Eeg Module, M-Eeg and Datex-Ohmeda Eeg Headbox, N-Eeg and Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Datex-Ohmeda, Inc.
- Decided: Jun 16, 2000 after 88 days
- Product code: OLT (Non-Normalizing Quantitative Electroencephalograph Software)
- Device class: 2
- Regulation: 21 CFR 882.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K051883: Datex-Ohmeda S/5 Eeg Module, E-Eeg and Datex-Ohmeda S/5 Eeg Headbox, N-Eeg and Accessories. (2005), 1 descendant of its own
- K191322: E-Eegx, N-Eegx (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K000892
Methodology: https://510kreport.com/methodology