K-number	K212208
Device name	Philips IntelliVue GuardianSoftware (Rev. E.0X)
Applicant	Philips Medizin Systeme Boeblingen GmbH
Product code	DXJ
Device class	Class II
Decision date	Sep 30, 2021
Decision	Substantially Equivalent
Regulation	870.2450

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View the full FDA submission: accessdata.fda.gov

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Philips IntelliVue GuardianSoftware (Rev. E.0X)

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