K-number	K203575
Device name	GlidePath Retro Long-Term Hemodialysis Catheter
Applicant	C.R. Bard, Inc.
Product code	MSD
Device class	Class II
Decision date	Jul 1, 2021
Decision	Unknown
Regulation	876.5540

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Source

View the full FDA submission: accessdata.fda.gov

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GlidePath Retro Long-Term Hemodialysis Catheter

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