Dashboard (P007000)
K-Number: K260211 · 2026-08-13
Device Summary
Frequently Asked Questions
What is the Dashboard (P007000)?
Dashboard (P007000) is a medical device that received FDA 510(k) clearance on 2026-08-13. The listed applicant is Hill-Rom, Inc.. The 510(k) number is K260211.
When did Dashboard (P007000) receive FDA 510(k) clearance?
Dashboard (P007000) received FDA 510(k) clearance on 2026-08-13, under 510(k) number K260211.
Who is the listed applicant for Dashboard (P007000)?
The FDA 510(k) record lists Hill-Rom, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dashboard (P007000)?
The FDA product code for Dashboard (P007000) is MSX.
Other records listing Hill-Rom, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MSX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.