K-number	K113398
Device name	NEXUS TKO-6, LUER-ACTIVATED DEVICE
Applicant	Nexus Medical, LLC
Product code	FPA
Device class	Class II
Decision date	Apr 18, 2012
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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NEXUS TKO-6, LUER-ACTIVATED DEVICE

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