# K060092: Quickcat Extraction Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Kensey Nash Corp.
- Decided: Mar 9, 2006 after 56 days
- Product code: QEZ (Aspiration Thrombectomy Catheter)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K010579 (2001). 10 ancestors in all.
2 later devices descend 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)
- K050276: Diver C.E. Catheter, Invatec Innovative Technologies, S.R.L. (2005) Summary page 1.
- K040869: Export Catheter, Medtronic Vascular (2004) Summary page 1.
- K032763: Vascular Solutions Pronto Extraction Catheter, Vascular Solutions, Inc. (2003) Summary page 1.

## Most influential descendants
- K073519: Quickcat Extraction Catheter, Model 60090-01 (2008), 1 descendant of its own
- K091703: HD Guide Catheter, Model 90019, 90022, 90023, 90120, 90121, 90130, 90131 (2009), 0 descendants of its own

## Recalls of this device
- Jul 1, 2010 · Not classified · Z-2190-2010: Guidewire lumen may be occluded, preventing guidewire insertion into the catheter.

## Indications for use
The QuickCatTM Extraction Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the arterial system.

Source page: https://510kreport.com/device/K060092
Methodology: https://510kreport.com/methodology