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FDA 510(k)

Venture 0.014 Catheter

K-Number: K182570 · 2019-03-13

ApplicantVascular Solutions, LLC
Decision Date2019-03-13
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Venture 0.014 Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, LLC. It received FDA 510(k) clearance on 2019-03-13 under 510(k) number K182570. 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 0.014 Catheter?

Venture 0.014 Catheter is a medical device that received FDA 510(k) clearance on 2019-03-13. The listed applicant is Vascular Solutions, LLC. The 510(k) number is K182570.

When did Venture 0.014 Catheter receive FDA 510(k) clearance?

Venture 0.014 Catheter received FDA 510(k) clearance on 2019-03-13, under 510(k) number K182570.

Who is the listed applicant for Venture 0.014 Catheter?

The FDA 510(k) record lists Vascular Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Venture 0.014 Catheter?

The FDA product code for Venture 0.014 Catheter is 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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