K-number	K895805
Device name	SLIDEX ROTA-KIT 2
Applicant	Vitek Systems, Inc.
Product code	LIQ
Device class	Class I
Decision date	Feb 26, 1991
Decision	Substantially Equivalent
Regulation	866.3405

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View the full FDA submission: accessdata.fda.gov

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SLIDEX ROTA-KIT 2

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