# K152335: Export Advance Aspiration Catheter

- Pathway: 510(k) (Special)
- Applicant: Medtronic, Inc.
- Decided: Sep 18, 2015 after 30 days
- Product code: DXE (Catheter, Embolectomy)
- 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 K010579 (2001). 11 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130536: Export Advance Aspiration Catheter, Medtronic, Inc. (2013) Summary page 4.

## Most influential descendants
- K253589: Liberant™ RX Aspiration Catheter (2026), 0 descendants of its own
- K190619: Aspiron (TM) Aspiration Catheter (2019), 0 descendants of its own

## Indications for use
The Export Advance™ Aspiration Catheter is indicated for: - Removal/aspiration of embolic material (thrombus/debris) from vessels of the arterial system, and - To sub selectively infuse/deliver diagnostics or therapeutics agents with or without vessel occlusion.

Source page: https://510kreport.com/device/K152335
Methodology: https://510kreport.com/methodology