K-number	K973702
Device name	ELECSYS VITAMIN B12 ASSAY
Applicant	Boehringer Mannheim Corp.
Product code	CDD
Device class	Class II
Decision date	Nov 13, 1997
Decision	Substantially Equivalent
Regulation	862.1810

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View the full FDA submission: accessdata.fda.gov

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ELECSYS VITAMIN B12 ASSAY

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