Class Class II

IntelliVue Patient Monitor MX750; IntelliVue Patient Monitor MX850; IntelliVue 4-Slot Module Rack FMX-4 (866471 866470 866468 ) (K251702)

K251702 2025-11-10 Traditional
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Description

IntelliVue Patient Monitor MX750; IntelliVue Patient Monitor MX850; IntelliVue 4-Slot Module Rack FMX-4 (866471 866470 866468 ) by Philips Medizin Systeme Böblingen GmbH, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251702
Clearance Date2025-11-10
Clearance TypeTraditional
Product CodeMHX
Regulation Number870.1025

Categories

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