K-number	K830646
Device name	DIRECTIGEN NEISSERIA MENINGITIDIS
Applicant	Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code	—
Device class	Class unclassified
Decision date	May 27, 1983
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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DIRECTIGEN NEISSERIA MENINGITIDIS

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