CLEARLUMEN THROMBECTOMY SYSTEM— 510(k) K140296

Name: FDA 510(k) clearance K140296
Creator: U.S. Food and Drug Administration
Published: 2014-12-02

Unknown

Walk Vascular, LLC

FDA 510(k) clearance K140296 for CLEARLUMEN THROMBECTOMY SYSTEM, Unknown on 2014-12-02. Applicant: Walk Vascular, LLC. Device class: 2.

Clearance details

Applicant: Walk Vascular, LLC
Product code: Code QEZ
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 2014-02-06
Decision date: 2014-12-02
Decision: Unknown
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code QEZ

product code QEZ

Death: 24
Total: 24

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.