# K000865: Quik-Cap

- Pathway: 510(k) (Traditional)
- Applicant: Neuroscan
- Decided: Apr 18, 2000 after 32 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
No predicates in its family tree.
20 later devices descend from it; 2 cite it directly.
0 of 21 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
- K071446: Electrode Array Cap (2008), 19 descendants of its own
- K110223: Waveguard (TM) Eeg Cap (2011), 18 descendants of its own
- K112319: Electro-Cap System (2012), 16 descendants of its own
- K200162: Disposable EEG Electrodes (MODEL: DL, E-CAP, FLEX-CAP) (2020), 9 descendants of its own
- K210805: Ceribell Instant EEG Headband (2021), 5 descendants of its own

Source page: https://510kreport.com/device/K000865
Methodology: https://510kreport.com/methodology