K-number	K131023
Device name	THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN
Applicant	Medical Products, LLC
Product code	NFB
Device class	Class II
Decision date	Oct 11, 2013
Decision	Substantially Equivalent
Regulation	868.5905

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View the full FDA submission: accessdata.fda.gov

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THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN

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