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FDA 510(k)

GlidePath 7.5F Long-Term Dialysis Catheter

K-Number: K202150 · 2020-11-18

ApplicantC.R. Bard, Inc.
Decision Date2020-11-18
Product CodeMSD
Advisory CommitteeGU
DecisionUnknown

Device Summary

GlidePath 7.5F Long-Term Dialysis Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2020-11-18 under approval number K202150. 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 7.5F Long-Term Dialysis Catheter?

GlidePath 7.5F Long-Term Dialysis Catheter is a medical device that received FDA 510(k) clearance on 2020-11-18. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K202150.

When was GlidePath 7.5F Long-Term Dialysis Catheter approved by the FDA?

GlidePath 7.5F Long-Term Dialysis Catheter received FDA 510(k) clearance on 2020-11-18, under approval number K202150.

What company makes GlidePath 7.5F Long-Term Dialysis Catheter?

GlidePath 7.5F Long-Term Dialysis Catheter is manufactured by C.R. Bard, Inc..

What is the FDA product code for GlidePath 7.5F Long-Term Dialysis Catheter?

The FDA product code for GlidePath 7.5F Long-Term Dialysis Catheter is MSD.

Related Clinical Trials

NCT05143164 Hydrocolloid Dressing for Catheter Exit Site Care in Peritoneal Dialysis Patients COMPLETED NCT07179705 Using a Hypotension Prediction Index to Prevent Low Blood Pressure During Dialysis in ICU Patients 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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