K-number	K162108
Device name	Pressio 2 ICP Monitoring System
Applicant	Sophysa SA
Product code	GWM
Device class	Class II
Decision date	Apr 17, 2017
Decision	Substantially Equivalent
Regulation	882.1620

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Source

View the full FDA submission: accessdata.fda.gov

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Pressio 2 ICP Monitoring System

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