K-number	K181311
Device name	Philips Hemodynamic Application R1.0
Applicant	Philips Medical Systems Nederlands B.V.
Product code	MWI
Device class	Class II
Decision date	Sep 7, 2018
Decision	Substantially Equivalent
Regulation	870.2300

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Source

View the full FDA submission: accessdata.fda.gov

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Philips Hemodynamic Application R1.0

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