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FDA 510(k)

IntelliVue Measurement Rack 6000 (867317)

K-Number: K253654 · 2026-03-30

ApplicantPhilips Medizin Systeme Böblingen GmbH
Decision Date2026-03-30
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IntelliVue Measurement Rack 6000 (867317) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. It received FDA 510(k) clearance on 2026-03-30 under approval number K253654. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IntelliVue Measurement Rack 6000 (867317)?

IntelliVue Measurement Rack 6000 (867317) is a medical device that received FDA 510(k) clearance on 2026-03-30. It is manufactured by Philips Medizin Systeme Böblingen GmbH. The 510(k) number is K253654.

When was IntelliVue Measurement Rack 6000 (867317) approved by the FDA?

IntelliVue Measurement Rack 6000 (867317) received FDA 510(k) clearance on 2026-03-30, under approval number K253654.

What company makes IntelliVue Measurement Rack 6000 (867317)?

IntelliVue Measurement Rack 6000 (867317) is manufactured by Philips Medizin Systeme Böblingen GmbH.

What is the FDA product code for IntelliVue Measurement Rack 6000 (867317)?

The FDA product code for IntelliVue Measurement Rack 6000 (867317) is MSX.

Other Devices by Philips Medizin Systeme Böblingen GmbH

K211900Patient Information Center iX K221348IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) K241556Cardiac Workstation (5000); Cardiac Workstation (7000) K251702IntelliVue Patient Monitor MX750; IntelliVue Patient Monitor MX850; IntelliVue 4-Slot Module Rack FMX-4 (866471 866470 866468 ) K250453IntelliVue Patient Monitor 6100 (6100); IntelliVue Patient Monitor 6300 (6300); IntelliVue Patient Monitor 6500 (6500) K242962Telemetry Monitor 5500 Release 4.0 (867232)

View all 9 devices →

Related Devices (Code: MSX)

K153156eCareManager 4.0.1Visicu, Inc. K160862AirStrip RPMAirstrip Technologies, Inc. K161164CareEvent inclusive of the CareEvent Mobile Application accessoryPhilips Medical Systems K171322eCareManager 4.1Visicu, Inc. K162607BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd. K180430Digistat Smart CentralAscom Ums Srl Unipersonale

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.

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