K-number	K092527
Device name	NEXUS INJECTION SITE, MODEL NIS-8
Applicant	Nexus Medical, LLC
Product code	FPA
Device class	Class II
Decision date	Feb 4, 2010
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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NEXUS INJECTION SITE, MODEL NIS-8

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