K-number	K133658
Device name	CDI BLOOD PARAMETER MONITORING SYSTEM 500
Applicant	Terumo Cardiovascular Systems Corp.
Product code	DRY
Device class	Class II
Decision date	Jul 25, 2014
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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