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FDA 510(k)

Sherlock 3CG+ T ip Confirmation System

K-Number: K180560 · 2018-06-18

ApplicantC.R. Bard, Inc.
Decision Date2018-06-18
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sherlock 3CG+ T ip Confirmation System is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2018-06-18 under approval number K180560. 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 Sherlock 3CG+ T ip Confirmation System?

Sherlock 3CG+ T ip Confirmation System is a medical device that received FDA 510(k) clearance on 2018-06-18. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K180560.

When was Sherlock 3CG+ T ip Confirmation System approved by the FDA?

Sherlock 3CG+ T ip Confirmation System received FDA 510(k) clearance on 2018-06-18, under approval number K180560.

What company makes Sherlock 3CG+ T ip Confirmation System?

Sherlock 3CG+ T ip Confirmation System is manufactured by C.R. Bard, Inc..

What is the FDA product code for Sherlock 3CG+ T ip Confirmation System?

The FDA product code for Sherlock 3CG+ T ip Confirmation System is LJS.

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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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