FDA 510(k)

GlidePath Retro Long-Term Hemodialysis Catheter

K-Number: K203575 · 2021-07-01

Decision Date2021-07-01

Product CodeMSD

Advisory CommitteeGU

DecisionUnknown

Device Summary

GlidePath Retro Long-Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2021-07-01 under 510(k) 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. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K203575.

When did GlidePath Retro Long-Term Hemodialysis Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for GlidePath Retro Long-Term Hemodialysis Catheter?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

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Related Devices (Code: MSD)

K241581Hemodialysis CatheterHaolang Medical USA Corporation K210461End CapMedical Components Inc (Medcomp)K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B Bard, Inc.K202150GlidePath 7.5F Long-Term Dialysis CatheterC.R. Bard, Inc.K202176Symetrex LTHD Catheter, Symetrex LTHD Catheter with SideholesMedical Components, Inc. (dba MedComp)

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.