K-number	K191245
Device name	Yumizen C1200 ALP, Yumizen C1200 Albumin
Applicant	HORIBA ABX SAS
Product code	CJE
Device class	Class II
Decision date	Aug 30, 2019
Decision	Substantially Equivalent
Regulation	862.1050

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Source

View the full FDA submission: accessdata.fda.gov

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Yumizen C1200 ALP, Yumizen C1200 Albumin

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