K-number	K896451
Device name	MODIFIED CEDIA(TM) CORTISOL ASSAY
Applicant	Microgenics Corp.
Product code	CGR
Device class	Class II
Decision date	Dec 12, 1989
Decision	Substantially Equivalent
Regulation	862.1205

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View the full FDA submission: accessdata.fda.gov

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MODIFIED CEDIA(TM) CORTISOL ASSAY

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