K-number	K980746
Device name	CEDIA DAU EDDP ASSAY
Applicant	Boehringer Mannheim Corp.
Product code	DJR
Device class	Class II
Decision date	May 26, 1998
Decision	Substantially Equivalent
Regulation	862.3620

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View the full FDA submission: accessdata.fda.gov

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CEDIA DAU EDDP ASSAY

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