# K240575: WaveGuard Net EEG Cap (NA-245, NA-255, NA-261, NA-265, NA-271, NA-281)

- Pathway: 510(k) (Traditional)
- Applicant: Eemagine Medical Imaging Solutions GmbH
- Decided: Nov 25, 2024 after 269 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K780045 (1978). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110223: Waveguard (TM) Eeg Cap, Eemagine Medical Imaging Solutions GmbH (2011) Summary page 5.

## Indications for use
This is an EEG electrode set intended for routine clinical settings where rapid placement of a large number of EEG electrodes is desired.

Source page: https://510kreport.com/device/K240575
Methodology: https://510kreport.com/methodology