# K060523: Neuroport Neural Signal Processing System

- Pathway: 510(k) (Special)
- Applicant: Cyberkinetics, Inc.
- Decided: Mar 28, 2006 after 29 days
- Product code: OMC (Reduced- Montage Standard Electroencephalograph)
- 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
Longest line of descent: 1 generation back to K042626 (2005). 1 ancestor in all.
9 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042626: Neuroport Neural Signal Processor (NSP) System, Cyberkinetics, Inc. (2005) Summary page 1.

## Most influential descendants
- K103140: Nicolet Wireless Eeg (2011), 7 descendants of its own
- K170441: ElectroTek (2017), 1 descendant of its own
- K162681: Enobio Wireless EEG (2017), 1 descendant of its own
- K151600: R-40 EEG  Amplifier (2015), 1 descendant of its own
- K261604: Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32) (2026), 0 descendants of its own

## Indications for use
The intended use of the Cyberkinetics Neurotechnology Systems, Inc. NeuroPort System is for temporary (< 30 days) recording and monitoring of brain electrical activity.

Source page: https://510kreport.com/device/K060523
Methodology: https://510kreport.com/methodology