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FDA 510(k)

GlidePath Retro Long-Term Hemodialysis Catheter

K-Number: K203575 · 2021-07-01

ApplicantC.R. Bard, Inc.
Decision Date2021-07-01
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

GlidePath Retro Long-Term Hemodialysis Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2021-07-01 under approval number K203575. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GlidePath Retro Long-Term Hemodialysis Catheter?

GlidePath Retro Long-Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2021-07-01. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K203575.

When was GlidePath Retro Long-Term Hemodialysis Catheter approved by the FDA?

GlidePath Retro Long-Term Hemodialysis Catheter received FDA 510(k) clearance on 2021-07-01, under approval number K203575.

What company makes GlidePath Retro Long-Term Hemodialysis Catheter?

GlidePath Retro Long-Term Hemodialysis Catheter is manufactured by C.R. Bard, Inc..

What is the FDA product code for GlidePath Retro Long-Term Hemodialysis Catheter?

The FDA product code for GlidePath Retro Long-Term Hemodialysis Catheter is MSD.

Related Clinical Trials

NCT07019610 Chlorhexidine Caps for CLABSI Prevention in Hemodialysis: a Pilot Randomized Controlled Trial NOT_YET_RECRUITING

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Related Devices (Code: MSD)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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