Dashboard (P007000)

FDA 510(k) K260211 · Hill-Rom, Inc.

Substantially Equivalent

510(k) numberK260211

Submission

Device name
Dashboard (P007000)
Applicant
Hill-Rom, Inc.
Batesville, IN, US
Received
January 23, 2026
Decision date
August 13, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MSX – System, Network And Communication, Physiological Monitors
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2300
Specialty
Cardiovascular
Life-sustaining
Yes

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Questions and answers

When was Dashboard (P007000) cleared by the FDA?

Dashboard (P007000) (K260211) received a 510(k) decision of Substantially Equivalent on August 13, 2026, 202 days after the submission was received.

What is the product code of K260211?

The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.