K-number	K092382
Device name	NEXUS PRESSURE RATED EXTENSION SETS
Applicant	Nexus Medical, LLC
Product code	FPA
Device class	Class II
Decision date	Apr 26, 2010
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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NEXUS PRESSURE RATED EXTENSION SETS

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