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FDA 510(k)

PowerPICC Provena Catheters with SOLO Valve Technology

K-Number: K162441 · 2017-04-24

ApplicantC.R. Bard, Inc.
Decision Date2017-04-24
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PowerPICC Provena Catheters with SOLO Valve Technology is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2017-04-24 under approval number K162441. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PowerPICC Provena Catheters with SOLO Valve Technology?

PowerPICC Provena Catheters with SOLO Valve Technology is a medical device that received FDA 510(k) clearance on 2017-04-24. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K162441.

When was PowerPICC Provena Catheters with SOLO Valve Technology approved by the FDA?

PowerPICC Provena Catheters with SOLO Valve Technology received FDA 510(k) clearance on 2017-04-24, under approval number K162441.

What company makes PowerPICC Provena Catheters with SOLO Valve Technology?

PowerPICC Provena Catheters with SOLO Valve Technology is manufactured by C.R. Bard, Inc..

What is the FDA product code for PowerPICC Provena Catheters with SOLO Valve Technology?

The FDA product code for PowerPICC Provena Catheters with SOLO Valve Technology is LJS.

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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

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Related Devices (Code: LJS)

K160925VPS Rhythm Device with TipTracker TechnologyArrow International, Inc. (A Subsidiary of Teleflex, Inc.) K162443PowerPICC Provena CathetersC.R. Bard, Inc. K161496Turbo-Flo PICC SetsCook Incorporated K161765CG+ Arrow JACCArrow International, Inc. (Subsidiary of Teleflex K153469Cathtong I PICC CatheterL&Z Us, Inc. K151985PowerPICC® EtOH Catheter and PowerPICC SOLO®2 EtOH CatheterC.R. Bard, Inc.

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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