K-number	K910210
Device name	SLIDEX MENINGITE-KIT 5
Applicant	Vitek Systems, Inc.
Product code	GTJ
Device class	Class II
Decision date	Aug 12, 1991
Decision	Substantially Equivalent
Regulation	866.3390

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View the full FDA submission: accessdata.fda.gov

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SLIDEX MENINGITE-KIT 5

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