FDA PMA

Stent, central venous

PMA Number: P980033 · 2026-05-06

ApplicantBoston Scientific Corporation

Decision Date2026-05-06

PMA NumberP980033

Product CodeQKJ

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeCV

Device Summary

Stent, central venous is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2026-05-06. The device is classified under product code QKJ. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Stent, central venous?

Stent, central venous is a medical device that received FDA 510(k) clearance on 2026-05-06. The listed applicant is Boston Scientific Corporation.

When did Stent, central venous receive FDA 510(k) clearance?

The clearance date for Stent, central venous can be found in the official FDA records.

Who is the listed applicant for Stent, central venous?

The FDA 510(k) record lists Boston Scientific Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stent, central venous?

The FDA product code for Stent, central venous is QKJ.

Related Clinical Trials

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.