# K072272: Honeywell Hommed Central Station 4.0

- Pathway: 510(k) (Special)
- Applicant: Honeywell Hommed, LLC
- Decided: Sep 7, 2007 after 23 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- 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 K053453 (2006). 1 ancestor in all.
3 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053453: Hommed Central Station, Version 3.5, Honeywell Hommed, LLC (2006) Summary page 1.

## Most influential descendants
- K120320: Connected Care Clinical Application (2012), 1 descendant of its own
- K153719: LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream (2016), 0 descendants of its own
- K131203: Ihealth Cloud (2013), 0 descendants of its own

## Indications for use
Central Station's intended use is to retrospectively receive, display and store monitored vital signs parameters and related data. Central Station displays the data and system alerts for review and interpretation by a healthcare professional. Central Station is not intended for emergency use or real-time monitoring.

Source page: https://510kreport.com/device/K072272
Methodology: https://510kreport.com/methodology