K-number	K150407
Device name	BioFlo Midline Catheter
Applicant	Navilyst Medical, Inc.
Product code	FOZ
Device class	Class II
Decision date	May 15, 2015
Decision	Substantially Equivalent
Regulation	880.5200

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Source

View the full FDA submission: accessdata.fda.gov

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BioFlo Midline Catheter

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