Class Class II

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) (K221348)

K221348 2023-02-03 Traditional
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Description

IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) by Philips Medizin Systeme Böblingen GmbH — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221348
Clearance Date2023-02-03
Clearance TypeTraditional
Product CodeMHX
Regulation Number870.1025

Categories

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