K-number	K961462
Device name	CEDIA THEOPHYLLINE ASSAY
Applicant	Boehringer Mannheim Corp.
Product code	KLS
Device class	Class II
Decision date	Jun 27, 1996
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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