# K053453: Hommed Central Station, Version 3.5

- Pathway: 510(k) (Traditional)
- Applicant: Honeywell Hommed, LLC
- Decided: May 5, 2006 after 144 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
No predicates in its family tree.
4 later devices descend from it; 1 cites 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)
- None. The FDA summary names its predicate without a number.
- (no number) HomMed Central Station: named in the summary without a submission number

## Most influential descendants
- K072272: Honeywell Hommed Central Station 4.0 (2007), 3 descendants of its own
- 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. The 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/K053453
Methodology: https://510kreport.com/methodology