# K072810: Pronto Low Profile (LP) Extraction Catheter, Model 5010

- Pathway: 510(k) (Traditional)
- Applicant: Vascular Solutions, Inc.
- Decided: Dec 19, 2007 after 79 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). 18 ancestors in all.
11 later devices descend from it; 1 cites it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052232: Vascular Solutions Pronto V3 Extraction Catheter, Vascular Solutions, Inc. (2005) Summary page 5.
- K063371: Pronto V3 Extraction Catheter, Model 5003, Vascular Solutions, Inc. (2006) Summary page 5.
- K071727: QXT Extraction Catheter, Vascular Solutions, Inc. (2007) Summary page 5.
- K051193: Vascular Solutions Pronto Short Extraction Catheter, Vascular Solutions, Inc. (2005)

## Most influential descendants
- K083784: Pronto V3 Extraction Center, Model 5003, Pronto LP Extraction Catheter, Model 5010, Skyway RX Support Catheter, (2009), 10 descendants of its own
- K103405: Pronto V4 Extraction Catheter 5.5F; Pronto V4 Extraction Catheter 6F; Pronto V4 Extraction 7F; Pronto V4 Extraction Cath (2010), 4 descendants of its own
- K161506: Penumbra Aspiration System (2016), 3 descendants of its own
- K163618: INDIGO Aspiration System (2017), 2 descendants of its own
- K162467: Twin-Pass Torque (2017), 2 descendants of its own

## Indications for use
The Pronto LP extraction catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the coronary and peripheral system.

Source page: https://510kreport.com/device/K072810
Methodology: https://510kreport.com/methodology