# K131998: Aspire RX-LP6 Aspiration Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Control Medical Technology, LLC
- Decided: Nov 26, 2013 after 151 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: 4 generations back to K010579 (2001). 11 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121301: Xpressway RX Catheter (6F LD-Verison), Kaneka Pharma America, LLC (2012) Summary page 5.
- K061958: Medtronic Export XT Catheter, Medtronic Vascular (2006) Summary page 5.
- K063371: Pronto V3 Extraction Catheter, Model 5003, Vascular Solutions, Inc. (2006) Summary page 5.
- (no number) Lumen – Volcano Xtract Aspiration Catheters: named in the summary without a submission number

## Most influential descendants
- K200629: Aspire Mechanical Aspirator G (2020), 0 descendants of its own

## Indications for use
The Aspire RX-LP6 Aspiration Catheter and Aspirator are indicated for the removal of fresh, soft emboli and thrombi from vessels in the coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K131998
Methodology: https://510kreport.com/methodology