K-number	K972962
Device name	3M CDI BLOOD PARAMETER MONITORING SYSTEM 500
Applicant	3M Company
Product code	DRY
Device class	Class II
Decision date	Nov 6, 1997
Decision	Substantially Equivalent
Regulation	870.4330

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View the full FDA submission: accessdata.fda.gov

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3M CDI BLOOD PARAMETER MONITORING SYSTEM 500

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