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)

Sherlock 3CG Tip Positioning System Stylet

K-Number: K172397 · 2017-09-29

ApplicantC.R. Bard, Inc.
Decision Date2017-09-29
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sherlock 3CG Tip Positioning System Stylet is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2017-09-29 under approval number K172397. 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 Tip Positioning System Stylet?

Sherlock 3CG Tip Positioning System Stylet is a medical device that received FDA 510(k) clearance on 2017-09-29. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K172397.

When was Sherlock 3CG Tip Positioning System Stylet approved by the FDA?

Sherlock 3CG Tip Positioning System Stylet received FDA 510(k) clearance on 2017-09-29, under approval number K172397.

What company makes Sherlock 3CG Tip Positioning System Stylet?

Sherlock 3CG Tip Positioning System Stylet is manufactured by C.R. Bard, Inc..

What is the FDA product code for Sherlock 3CG Tip Positioning System Stylet?

The FDA product code for Sherlock 3CG Tip Positioning System Stylet is LJS.

Related Clinical Trials

NCT03280862 DANISH-CRT - Does Electric Targeted LV Lead Positioning Improve Outcome in Patients With Heart Failure and Prolonged QRS COMPLETED NCT06795763 Acolyte CTO-PCI Study: Imaging and Catheter System to Treat Patients With Coronary Chronic Total Occlusion, Who Have Persistent Symptoms Following Medical Therapy and Are Undergoing Percutaneous Coronary Interventional Procedures ENROLLING_BY_INVITATION NCT07580651 Quality and Safety of Real-Time Brachytherapy Treatments: Clinical Implementation of a Multipoint Scintillation Detector for Treatment Monitoring NOT_YET_RECRUITING NCT06631638 EMPHASYS Cup Positioning in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN)) RECRUITING NCT00102544 Use of Tracking Devices to Locate Abnormalities During Invasive Procedures ENROLLING_BY_INVITATION NCT05776030 Multi-speed Ergonomic Wheelchair 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: 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.

↑