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FDA 510(k)

PowerGlide Pro™ Midline Catheter

K-Number: K240359 · 2024-07-29

ApplicantBecton, Dickinson and Company (Bard Access Systems, Inc.)
Decision Date2024-07-29
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PowerGlide Pro™ Midline Catheter is a medical device manufactured by Becton, Dickinson and Company (Bard Access Systems, Inc.). It received FDA 510(k) clearance on 2024-07-29 under approval number K240359. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PowerGlide Pro™ Midline Catheter?

PowerGlide Pro™ Midline Catheter is a medical device that received FDA 510(k) clearance on 2024-07-29. It is manufactured by Becton, Dickinson and Company (Bard Access Systems, Inc.). The 510(k) number is K240359.

When was PowerGlide Pro™ Midline Catheter approved by the FDA?

PowerGlide Pro™ Midline Catheter received FDA 510(k) clearance on 2024-07-29, under approval number K240359.

What company makes PowerGlide Pro™ Midline Catheter?

PowerGlide Pro™ Midline Catheter is manufactured by Becton, Dickinson and Company (Bard Access Systems, Inc.).

What is the FDA product code for PowerGlide Pro™ Midline Catheter?

The FDA product code for PowerGlide Pro™ Midline Catheter is FOZ.

Related Clinical Trials

NCT07610681 Midline Catheter Study ACTIVE_NOT_RECRUITING NCT06958731 In-plane Versus Real Time Bi-plane Single-operator Laser-assisted With a Innovative T-shaped Probe for Ultrasound-guided Internal Jugular Vein Catheterization:A Randomized Controlled Trial ENROLLING_BY_INVITATION NCT06979167 Complications of Midline Catheter in Surgical Children COMPLETED NCT06770374 Effectiveness of a Zinc Oxide Adhesive Securement Device in the Fixation of Midline and Peripherally Inserted Central Catheters in Hospitalized Adult Patients RECRUITING NCT06884176 CVCs Versus Midline Catheters NOT_YET_RECRUITING

Related Devices (Code: FOZ)

K162894AccuCath Intravascular CatheterC.R. Bard, Inc. K161779MedSource TrueSafe Safety IV Catheter, MedSource TrueSafe Comfort Safety IV CatheterMedsource International, LLC K162377PowerGlide Pro Midline CatheterC.R. Bard, Inc. K161866BioFlo Midline CatheterNavilyst Medical, Inc. K161777BD Nexiva and BD Nexiva Diffusics Closed IV Catheter SystemsBecton Dickinson Infusion Therapy Systems, Inc. K160592SUPERCATH 6Togo Medikit Co., Ltd.

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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