# K240397: AlphaVac MMA F1885 System (H787253020)

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: Apr 1, 2024 after 52 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: 5 generations back to K832023 (1983). 18 ancestors in all.
No later device cites it as a predicate yet.
3 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180466: FlowTriever Retrieval/Aspiration System, Inari Medical, Inc. (2018) Summary page 5.

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

Source page: https://510kreport.com/device/K240397
Methodology: https://510kreport.com/methodology