K-number	K123039
Device name	CDI BLOOD PARAMETER MONITORING SYSTEM 500
Applicant	Terumo Cardiovascular Systems Corp.
Product code	DRY
Device class	Class II
Decision date	Nov 20, 2012
Decision	Substantially Equivalent
Regulation	870.4330

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Source

View the full FDA submission: accessdata.fda.gov

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CDI BLOOD PARAMETER MONITORING SYSTEM 500

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