K-number	K130416
Device name	NEXUS TKO-6P LUER ACTIVATED DEVICE
Applicant	Nexus Medical, LLC
Product code	FPA
Device class	Class II
Decision date	Jun 12, 2013
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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NEXUS TKO-6P LUER ACTIVATED DEVICE

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