FDA PMA

Stent, iliac vein

PMA Number: P180037 · 2026-06-10

ApplicantBard Peripheral Vascular, Inc.

Decision Date2026-06-10

PMA NumberP180037

Product CodeQAN

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeCV

Device Summary

Stent, iliac vein 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 2026-06-10. The device is classified under product code QAN. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Stent, iliac vein?

Stent, iliac vein is a medical device that received FDA 510(k) clearance on 2026-06-10. The listed applicant is Bard Peripheral Vascular, Inc..

When did Stent, iliac vein receive FDA 510(k) clearance?

The clearance date for Stent, iliac vein can be found in the official FDA records.

Who is the listed applicant for Stent, iliac vein?

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 Stent, iliac vein?

The FDA product code for Stent, iliac vein is QAN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.