Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PowerGlide ST Midline Catheter

K-Number: K170158 · 2017-06-01

ApplicantC.R. Bard, Inc.
Decision Date2017-06-01
Product CodePND
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PowerGlide ST Midline Catheter is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2017-06-01 under approval number K170158. The device is classified under product code PND. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PowerGlide ST Midline Catheter?

PowerGlide ST Midline Catheter is a medical device that received FDA 510(k) clearance on 2017-06-01. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K170158.

When was PowerGlide ST Midline Catheter approved by the FDA?

PowerGlide ST Midline Catheter received FDA 510(k) clearance on 2017-06-01, under approval number K170158.

What company makes PowerGlide ST Midline Catheter?

PowerGlide ST Midline Catheter is manufactured by C.R. Bard, Inc..

What is the FDA product code for PowerGlide ST Midline Catheter?

The FDA product code for PowerGlide ST Midline Catheter is PND.

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

Other Devices by C.R. Bard, Inc.

K162900PowerMidline Catheter K162894AccuCath Intravascular Catheter K162769Pinpoint GT Introducer Needle K162443PowerPICC Provena Catheters K161424Phasix Mesh K162377PowerGlide Pro Midline Catheter

View all 67 devices →

Related Devices (Code: PND)

K162900PowerMidline CatheterC.R. Bard, Inc. K161313ARROW Pressure Injectable Midline Catheter with Chlorag+ard Antimicrobial and Antithrombogenic TechnologyArrow International, Inc. (Subsidiary of Teleflex, Inc.) K153393PowerMidline CatheterC.R. Bard, Inc. K171483ArchFlo CT MidlineMedcomp (Dba Medical Components, Inc.) K170770CT MidlineMedical Components, Inc. (dba MedComp) K181208Vygon Midline 3 Fr SL Catheter; Vygon Midline 4 Fr SL Catheter; Vygon Midline 5 Fr DL CatheterVygon USA

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.

↑