K-number	K081920
Device name	BD GENEOHM CDIFF ASSAY
Applicant	Bd Diagnostics (Geneohm Sciences, Inc.)
Product code	LLH
Device class	Class I
Decision date	Dec 19, 2008
Decision	Substantially Equivalent
Regulation	866.2660

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Source

View the full FDA submission: accessdata.fda.gov

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BD GENEOHM CDIFF ASSAY

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