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FDA 510(k)

GuideLiner V3 Catheter

K-Number: K172090 · 2017-10-20

ApplicantVascular Solutions, Inc.
Decision Date2017-10-20
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GuideLiner V3 Catheter is a medical device manufactured by Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2017-10-20 under approval number K172090. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GuideLiner V3 Catheter?

GuideLiner V3 Catheter is a medical device that received FDA 510(k) clearance on 2017-10-20. It is manufactured by Vascular Solutions, Inc.. The 510(k) number is K172090.

When was GuideLiner V3 Catheter approved by the FDA?

GuideLiner V3 Catheter received FDA 510(k) clearance on 2017-10-20, under approval number K172090.

What company makes GuideLiner V3 Catheter?

GuideLiner V3 Catheter is manufactured by Vascular Solutions, Inc..

What is the FDA product code for GuideLiner V3 Catheter?

The FDA product code for GuideLiner V3 Catheter is DQY.

Other Devices by Vascular Solutions, Inc.

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Related Devices (Code: DQY)

K163000AMPLATZER TorqVue 45x45 Delivery SheathAga Medical COrporation (Wholly Owned by St. Jude Medical CO K160561Boosting CatheterQxmedical, LLC K161546R2P SlenGuideAshitaka Factory of Terumo Corporation K161152Navien Intracranial Support CatheterMicro Therapeutics, Inc. d/b/a ev3 Neurovascular K162384TrailBlazer Angled Support CatheterMedtronic Vascular, Inc.(Formerly Ev3 Inc.) K162359Surefire Guiding CatheterSurefire Medical, 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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