K-number	K884358
Device name	CEDIA THEOPHYLLINE ASSAY
Applicant	Microgenics Corp.
Product code	KLS
Device class	Class II
Decision date	Feb 7, 1989
Decision	Substantially Equivalent
Regulation	862.3880

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View the full FDA submission: accessdata.fda.gov

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CEDIA THEOPHYLLINE ASSAY

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