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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 the device name listed in this FDA 510(k) record. The listed applicant is Bard Peripheral Vascular, Inc.. It received FDA 510(k) clearance on 2022-05-31 under 510(k) 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. The listed applicant is Bard Peripheral Vascular, Inc.. The 510(k) number is K221440.

When did Liverty™ TIPS Access Set receive FDA 510(k) clearance?

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

Who is the listed applicant for Liverty™ TIPS Access Set?

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

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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Related Devices (Code: 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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