# K151006: EarlySense Central Display Station (CDS)

- Pathway: 510(k) (Traditional)
- Applicant: Earlysense, Ltd.
- Decided: Aug 31, 2015 after 138 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: 6 generations back to K925411 (1993). 14 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121885: Earlysense Central Display System, Earlysense, Ltd. (2012) Summary page 4.
- K132807: Monitoring Station, Connex (R) Central Station (CS), Welch Allyn, Inc. (2014) Summary page 4.

## Most influential descendants
- 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 Central Display System is intended to provide remote central monitoring and display of information as recorded by multiple EarlySense bedside units, on a central remote screen. The system can be used in hospitals or hospital type and clinic environment.

Source page: https://510kreport.com/device/K151006
Methodology: https://510kreport.com/methodology