# K052232: Vascular Solutions Pronto V3 Extraction Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Vascular Solutions, Inc.
- Decided: Sep 28, 2005 after 42 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
No predicates in its family tree.
33 later devices descend from it; 4 cite it directly.
1 of 34 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Vascular Solutions, Inc. Pronto Extraction Catheter: named in the summary without a submission number
- (no number) Medtronic Export™ Aspiration Catheter: named in the summary without a submission number

## Most influential descendants
- K063371: Pronto V3 Extraction Catheter, Model 5003 (2006), 27 descendants of its own
- K071727: QXT Extraction Catheter (2007), 12 descendants of its own
- K072810: Pronto Low Profile (LP) Extraction Catheter, Model 5010 (2007), 11 descendants of its own
- K083784: Pronto V3 Extraction Center, Model 5003, Pronto LP Extraction Catheter, Model 5010, Skyway RX Support Catheter, (2009), 10 descendants of its own
- K053372: Lbi Catheter System (2006), 10 descendants of its own

## Indications for use
The Pronto V3 Extraction Catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels of the arterial systems.

Source page: https://510kreport.com/device/K052232
Methodology: https://510kreport.com/methodology