Class Class II

IntelliVue Patient Monitor 6100 (6100); IntelliVue Patient Monitor 6300 (6300); IntelliVue Patient Monitor 6500 (6500) (K250453)

K250453 2025-09-02 Traditional
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Description

IntelliVue Patient Monitor 6100 (6100); IntelliVue Patient Monitor 6300 (6300); IntelliVue Patient Monitor 6500 (6500) by Philips Medizin Systeme Böblingen GmbH, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250453
Clearance Date2025-09-02
Clearance TypeTraditional
Product CodeMHX
Regulation Number870.1025

Categories

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