K-number	K182110
Device name	CDI Blood Parameter Monitoring System 550
Applicant	Terumo Cardiovascular Systems Corporation
Product code	DRY
Device class	Class II
Decision date	Nov 2, 2018
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 550

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