# K172866: NeuroCap

- Pathway: 510(k) (Traditional)
- Applicant: Memory MD, Inc.
- Decided: Apr 27, 2018 after 219 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: 1 generation back to K092828 (2010). 1 ancestor in all.
1 later device descends 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)
- K092828: Statnet, Model 3100, Hydrodot, Inc. (2010) Summary page 4.

## Most influential descendants
- K202913: NeuroCap (Model DEC22) (2021), 0 descendants of its own

## Indications for use
The NeuroCap (model DEC18) is an Electroencephalogram (EEG) electrode array intended for use in ER (emergency room), ICU (intensive care unit) and OR (operating room) for recording of STAT EEGs in patients of 18 years of age and older.

Source page: https://510kreport.com/device/K172866
Methodology: https://510kreport.com/methodology