# K121885: Earlysense Central Display System

- Pathway: 510(k) (Special)
- Applicant: Earlysense, Ltd.
- Decided: Sep 10, 2012 after 74 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
Longest line of descent: 3 generations back to K061932 (2006). 4 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110521: Everon Central Display Station (CDS), Earlysense, Ltd. (2011)

## Most influential descendants
- 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
- K243837: iBSM (2025), 0 descendants of its own
- K212622: Zyter RPM (2022), 0 descendants of its own

## Indications for use
The EarlySense (Ever~n) Central Display Station (CDS) is intended to provide secondary display of the information as displayed on multiple individual bed side monitoring units, on a central remote screen. The EarlySense.(Ever~n) CDS is not intended to replace any part of the bed-side patient monitoring procedures. The system can be used in hospitals or hospital type and clinic environment.

Source page: https://510kreport.com/device/K121885
Methodology: https://510kreport.com/methodology