K-number	K896021
Device name	CEDIA DIGITOXIN ASSAY
Applicant	Microgenics Corp.
Product code	LFM
Device class	Class II
Decision date	Nov 8, 1989
Decision	Substantially Equivalent
Regulation	862.3300

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View the full FDA submission: accessdata.fda.gov

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CEDIA DIGITOXIN ASSAY

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