K-number	K173941
Device name	IntelliSpace Perinatal Rev.K.00
Applicant	Philips Medizin Systeme Boeblingen GmbH
Product code	HGM
Device class	Class II
Decision date	Sep 10, 2018
Decision	Substantially Equivalent
Regulation	884.2740

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Source

View the full FDA submission: accessdata.fda.gov

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IntelliSpace Perinatal Rev.K.00

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