K-number	K162377
Device name	PowerGlide Pro Midline Catheter
Applicant	C.R. Bard, Inc.
Product code	FOZ
Device class	Class II
Decision date	Sep 22, 2016
Decision	Substantially Equivalent
Regulation	880.5200

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Source

View the full FDA submission: accessdata.fda.gov

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PowerGlide Pro Midline Catheter

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