AlphaVac Multipurpose Mechanical Aspiration System F1885— 510(k) K252509

Name: FDA 510(k) clearance K252509
Creator: U.S. Food and Drug Administration
Published: 2025-11-24

Substantially Equivalent

AngioDynamics, Inc.

FDA 510(k) clearance K252509 for AlphaVac Multipurpose Mechanical Aspiration System F1885, Substantially Equivalent on 2025-11-24. Applicant: AngioDynamics, Inc.. Device class: 2.

Clearance details

Applicant: AngioDynamics, Inc.
Product code: Code QEZ
Device class: Class 2
Regulation: 21 CFR 870.5150
Advisory panel: Cardiovascular
Date received: 2025-08-08
Decision date: 2025-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Queensburgy, NY, 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.