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FDA 510(k)

Twin-Pass Dual Access Catheter

K-Number: K193119 · 2020-06-29

ApplicantVascular Solutions, LLC
Decision Date2020-06-29
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Twin-Pass Dual Access Catheter is a medical device manufactured by Vascular Solutions, LLC. It received FDA 510(k) clearance on 2020-06-29 under approval number K193119. 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 Twin-Pass Dual Access Catheter?

Twin-Pass Dual Access Catheter is a medical device that received FDA 510(k) clearance on 2020-06-29. It is manufactured by Vascular Solutions, LLC. The 510(k) number is K193119.

When was Twin-Pass Dual Access Catheter approved by the FDA?

Twin-Pass Dual Access Catheter received FDA 510(k) clearance on 2020-06-29, under approval number K193119.

What company makes Twin-Pass Dual Access Catheter?

Twin-Pass Dual Access Catheter is manufactured by Vascular Solutions, LLC.

What is the FDA product code for Twin-Pass Dual Access Catheter?

The FDA product code for Twin-Pass Dual Access Catheter is DQY.

Related Clinical Trials

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Related Devices (Code: DQY)

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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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