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Philips MP5 Intellivue Patient Monitor

FDA 510(k)

Class II (US FDA 510(k))

510(k) K062392

by Philips Medizin Systeme Boeblingen GmbH

Identifiers

510(k) Number
K062392 FDA 510(k)
FDA Product Code
MHX FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 870.1025 FDA 510(k)
Regulation Number
870.1025 FDA 510(k)
Advisory Committee
Cardiovascular FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

The Philips Mp5 Intellivue Patient Monitor is a physiological patient monitor with arrhythmia detection or alarms. It is designed to provide monitoring power and functionality in a compact and rugged housing, serving a wide range of care environments. The device is classified as a Monitor, Physiological, Patient, and is used to deliver actionable information about patients.

The Philips Mp5 Intellivue Patient Monitor is supplied with a product code of MHX and a regulation number of 870.1025. It has been authorized with an FDA 510K clearance, and the decision description is Substantially Equivalent. The device is intended for use in cardiovascular medical specialties, and its storage and use are subject to standard medical device protocols.

This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: Philips - IntelliVue MP5 Portable patient monitor - Philips, Philips - IntelliVue MP5 Bettseitiger Patientenmonitor - Philips, Philips - IntelliVue MP5 Portable patient monitor, PDF Compact, flexible confidence - Philips

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Philips Medizin Systeme Boeblingen GmbH

Sources (1)

  • FDA 510(k) K062392 24 fields · synced Oct 6, 2026