K-number	K972963
Device name	MODIFIED CEDIA DAU PCP ASSAY
Applicant	Boehringer Mannheim Corp.
Product code	LCM
Device class	Class U
Decision date	Sep 22, 1997
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MODIFIED CEDIA DAU PCP ASSAY

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