# K213388: AlphaVac Multipurpose Mechanical Aspiration (MMA) F1885 System

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: Apr 4, 2022 after 172 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K832023 (1983). 20 ancestors in all.
No later device cites it as a predicate yet.
3 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211081: AlphaVac Multipurpose Mechanical Aspiration (MMA) System, AngioDynamics, Inc. (2021) Summary page 4.

## Indications for use
The Cannula is indicated for * the non-surgical removal of thrombi or emboli from venous vasculature. * aspiration of contrast media and other fluids from venous vasculature. The Cannula is intended for use in the venous system. The Handle is indicated as a vacuum source for the AlphaVac MMA System.

Source page: https://510kreport.com/device/K213388
Methodology: https://510kreport.com/methodology