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FDA 510(k)

Venture 038 catheter

K-Number: K171335 · 2017-06-07

ApplicantVascular Solutions, Inc.
Decision Date2017-06-07
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Venture 038 catheter is a medical device manufactured by Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2017-06-07 under approval number K171335. 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 Venture 038 catheter?

Venture 038 catheter is a medical device that received FDA 510(k) clearance on 2017-06-07. It is manufactured by Vascular Solutions, Inc.. The 510(k) number is K171335.

When was Venture 038 catheter approved by the FDA?

Venture 038 catheter received FDA 510(k) clearance on 2017-06-07, under approval number K171335.

What company makes Venture 038 catheter?

Venture 038 catheter is manufactured by Vascular Solutions, Inc..

What is the FDA product code for Venture 038 catheter?

The FDA product code for Venture 038 catheter is DQY.

Other Devices by Vascular Solutions, Inc.

K161702Endura guidewire K162272Fluent inflation device K161336VSI StraitSet micro-introducer kit K173532Raider Guidewire K173266Octane aspiration system K170544Langston dual lumen catheter

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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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