Class Class II

IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) (K252726)

K252726 2026-02-06 Traditional
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Description

IntelliVue Multi-Measurement Module X3 (867030); IntelliVue Patient Monitor MX100 (867033); IntelliVue MMX (867036) by Philips Medizin Systeme Boeblingen GmbH, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252726
Clearance Date2026-02-06
Clearance TypeTraditional
Product CodeMHX
Regulation Number870.1025

Categories

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