meddevicedb.com FDA Device Reference

AlphaVac Multipurpose Mechanical Aspiration System F1885

K252509 Class II Traditional
Decision Date
2025-11-24
Sponsor / Applicant
AngioDynamics, Inc.

Technical Specification

510(k) Submission ID K252509
Product Code QEZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2025-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AlphaVac Multipurpose Mechanical Aspiration System F1885 received FDA 510(k) clearance under submission number K252509, sponsored by AngioDynamics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code QEZ and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.