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FDA 510(k)

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470)

K-Number: K221348 · 2023-02-03

ApplicantPhilips Medizin Systeme Böblingen GmbH
Decision Date2023-02-03
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. It received FDA 510(k) clearance on 2023-02-03 under approval number K221348. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470)?

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) is a medical device that received FDA 510(k) clearance on 2023-02-03. It is manufactured by Philips Medizin Systeme Böblingen GmbH. The 510(k) number is K221348.

When was IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) approved by the FDA?

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) received FDA 510(k) clearance on 2023-02-03, under approval number K221348.

What company makes IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470)?

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) is manufactured by Philips Medizin Systeme Böblingen GmbH.

What is the FDA product code for IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470)?

The FDA product code for IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) is MHX.

Related Clinical Trials

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Related PubMed Literature

PMID: 28216355 Innovative postmarket device evaluation using a quality registry to monitor thoracic endovascular aortic repair in the treatment of aortic dissection. Journal of vascular surgery (2017)

Other Devices by Philips Medizin Systeme Böblingen GmbH

K211900Patient Information Center iX 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) K241890Philips Holter Analysis System

View all 9 devices →

Related Devices (Code: MHX)

K160981Patient MonitorEdan Instruments, Inc. K153707Nihon Kohden Vital Sign TelemeterNihon Kohden Corporation K160685Surveyor S4 Mobile MonitorMortara Instrument, Inc. K161531IntelliVue Patient Monitors MP2, MP5, MP5T, MP5SC, and Multi-Measurement Module X2; IntelliVue Patient Monitors MP20, MP30, MP40, MP50, MP60; IntelliVue Patient Monitors MP70, MP80, MP90;IntelliVue Patient Monitors MX400, MX430, MX450, MX500, MX550, MX600;IntelliVue Patient Monitors MX700, MX800Philips Medizin Systeme Boeblingen GmbH K153702M3290B Philips IntelliVue Information Center iXPhilips Medical Systems K160951Philips Efficia CMS200 Central Monitoring SystemPhilips Medical Systems

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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