# K100376: Everon Central Display Station - CDS, Model Version 1.0.0

- Pathway: 510(k) (Traditional)
- Applicant: Earlysense, Ltd.
- Decided: Aug 6, 2010 after 175 days
- Product code: MSX (System, Network And Communication, Physiological Monitors)
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K110521: Everon Central Display Station (CDS) (2011), 6 descendants of its own
- K121885: Earlysense Central Display System (2012), 5 descendants of its own
- K151006: EarlySense Central Display Station (CDS) (2015), 4 descendants of its own
- K202497: Aulisa Multiple Patient Digital Vital Sign Monitoring System (2020), 2 descendants of its own
- K242842: ANNE View, Central Hub (2025), 1 descendant of its own

Source page: https://510kreport.com/device/K100376
Methodology: https://510kreport.com/methodology