K-number	K192028
Device name	Yumizen C1200 CRP
Applicant	HORIBA ABX SAS
Product code	DCK
Device class	Class II
Decision date	Jun 25, 2020
Decision	Substantially Equivalent
Regulation	866.5270

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Source

View the full FDA submission: accessdata.fda.gov

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Yumizen C1200 CRP

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