K-number	K131085
Device name	CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000
Applicant	Mespere Lifesciences, Inc.
Product code	PFA
Device class	Class II
Decision date	Aug 22, 2013
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000

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