FDA 510(k)

GlidePath 7.5F Long-Term Dialysis Catheter

K-Number: K202150 · 2020-11-18

Decision Date2020-11-18

Product CodeMSD

Advisory CommitteeGU

DecisionUnknown

Device Summary

GlidePath 7.5F Long-Term Dialysis 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 2020-11-18 under 510(k) 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. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K202150.

When did GlidePath 7.5F Long-Term Dialysis Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for GlidePath 7.5F Long-Term Dialysis 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 7.5F Long-Term Dialysis Catheter?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT03911700Prophylactic Reinforcement of Ventral Abdominal Incisions TrialACTIVE_NOT_RECRUITING NCT04634916Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF SystemRECRUITING NCT05711316The BD Liverty™ TIPS Stent Graft StudyACTIVE_NOT_RECRUITING NCT05945329Study of GalaFLEX LITE™ Scaffold in Treatment of Capsular Contracture After Breast Implant AugmentationRECRUITING NCT07282860An Evaluation of the PureWick™ Male External Catheter Versus an Established Comparator Overnight in the Home Setting for Incontinence in Adult MalesCOMPLETED NCT07744945Evaluation of Male and Female External Catheters for Urine Output Monitoring in the ICUNOT_YET_RECRUITING

Other records listing C.R. Bard, Inc. as applicant

PMA P800002Agent, absorbable hemostatic, collagen based K253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric Tube - 20 French (0092100); Blakemore Esophageal-Nasogastric Tube - 16 French (0092300)PMA P170042System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment K254076BD Touchless™ Plus Unisex Pre-Lubricated Urethral Catheter Kit K252971Elyra™ Thulium Fiber Laser System and Elyra™ Plus Thulium Fiber Laser System (Laser, Fibers, and Accessories)K251864Rubber Utility Catheter

View all 74 devices →

Related Devices (Code: MSD)

K241581Hemodialysis CatheterHaolang Medical USA Corporation K210461End CapMedical Components Inc (Medcomp)K203575GlidePath Retro Long-Term Hemodialysis CatheterC.R. Bard, Inc.K211410GlidePath 13F Long-Term Hemodialysis CatheterBard Peripheral Vascular, Inc.K203767Pristine Long-Term Hemodialysis CatheterC B 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.