Dashboard (P007000)— 510(k) K260211
Substantially EquivalentHill-Rom, Inc.
FDA 510(k) clearance K260211 for Dashboard (P007000), Substantially Equivalent on 2026-08-13. Applicant: Hill-Rom, Inc.. Device class: 2.
Summary
Hill-Rom's Dashboard, listed as P007000, is filed under product code MSX, physiological monitor network and communication systems. The record doesn't describe it beyond the name and that code.
Class II, 21 CFR 870.2300. Cardiovascular is both the classification panel and the review panel. It came in as a Traditional 510(k).
Hill-Rom filed from Batesville, Indiana. Review took 202 calendar days (January 23 to August 13, 2026) and ended in a substantially equivalent decision.
Clearance details
- Applicant
- Hill-Rom, Inc.
- Product code
- Product code MSX
- Device class
- Class 2
- Regulation
- 21 CFR 870.2300
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Batesville, IN, US
Recent devices under product code MSX
view allMore clearances from Hill-Rom, Inc.
view all- K202018 — Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Activation
- K180079 — Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Activation
- K013709 — HILL-ROM PRIMAVIEW MONITOR SYSTEM
- K973705 — CONTOR TABLE SURFACE
- K981081 — BRIGHTSTAR
Adverse events under product code MSX
product code MSX- Death
- 59
- Total
- 59
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.