FDA PMA

Pulmonary stent

PMA Number: P220004 · 2024-09-05

ApplicantCordis US Corp

Decision Date2024-09-05

PMA NumberP220004

Product CodeQWC

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeCV

Device Summary

Pulmonary stent is the device name listed in this FDA 510(k) record. The listed applicant is Cordis US Corp. It received FDA 510(k) clearance on 2024-09-05. The device is classified under product code QWC. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Pulmonary stent?

Pulmonary stent is a medical device that received FDA 510(k) clearance on 2024-09-05. The listed applicant is Cordis US Corp.

When did Pulmonary stent receive FDA 510(k) clearance?

The clearance date for Pulmonary stent can be found in the official FDA records.

Who is the listed applicant for Pulmonary stent?

The FDA 510(k) record lists Cordis US Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pulmonary stent?

The FDA product code for Pulmonary stent is QWC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

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.