K-number	K240359
Device name	PowerGlide Pro Midline Catheter
Applicant	Becton, Dickinson and Company (Bard Access Systems, Inc.)
Product code	FOZ
Device class	Class II
Decision date	Jul 29, 2024
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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PowerGlide Pro Midline Catheter