# K260211: Dashboard (P007000)

- Pathway: 510(k) (Traditional)
- Applicant: Hill-Rom, Inc.
- Decided: Aug 13, 2026 after 202 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: 32 generations back to K941811 (1994). 194 ancestors in all.
No later device cites it as a predicate yet.
0 of 195 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242750: Central Station, Nihon Kohden Digital Health Solutions, LLC (2025) Summary page 5.

## Indications for use
The Dashboard is a software product indicated for use as a secondary, visual communication tool for clinical caregivers within a healthcare environment. Dashboard displays EMR data, patient location, and alarm information received from Baxter devices. The information is presented on a monitor to allow patient status and device status to be readily viewable by clinical caregivers. The Dashboard does not replace the primary monitoring, alarm, or clinical assessment functions of the connected source devices.

Source page: https://510kreport.com/device/K260211
Methodology: https://510kreport.com/methodology