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FDA 510(k)

Liverty™ TIPS Access Set

K-Number: K221440 · 2022-05-31

ApplicantBard Peripheral Vascular, Inc.
Decision Date2022-05-31
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Liverty™ TIPS Access Set is a medical device manufactured by Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2022-05-31 under approval number K221440. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Liverty™ TIPS Access Set?

Liverty™ TIPS Access Set is a medical device that received FDA 510(k) clearance on 2022-05-31. It is manufactured by Bard Peripheral Vascular, Inc.. The 510(k) number is K221440.

When was Liverty™ TIPS Access Set approved by the FDA?

Liverty™ TIPS Access Set received FDA 510(k) clearance on 2022-05-31, under approval number K221440.

What company makes Liverty™ TIPS Access Set?

Liverty™ TIPS Access Set is manufactured by Bard Peripheral Vascular, Inc..

What is the FDA product code for Liverty™ TIPS Access Set?

The FDA product code for Liverty™ TIPS Access Set is DYB.

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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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