K-number	K161767
Device name	Philips IntelliVue GuardianSoftware
Applicant	Philips Medizin Systeme Boeblingen GmbH
Product code	DXJ
Device class	Class II
Decision date	Jan 27, 2017
Decision	Substantially Equivalent
Regulation	870.2450

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Source

View the full FDA submission: accessdata.fda.gov

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Philips IntelliVue GuardianSoftware

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