# K120707: Switch-IT Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Vascular Solutions, Inc.
- Decided: May 15, 2012 after 68 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K001992 (2000). 21 ancestors in all.
No later device cites it as a predicate yet.
1 of 22 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112082: Guideliner V2 Catheter, Vascular Solutions, Inc. (2011) Summary page 1.
- K101659: Supercross Microcatheter (130 CM), Supercross Microcatheter (150 CM) Model 5300, 5301, Vascular Solutions, Inc. (2010) Summary page 1.

## Indications for use
The Switch-it catheter is intended to be used in conjunction with guide catheters to facilitate placement and exchange of guidewires in the discrete coronary and peripheral vasculature.

Source page: https://510kreport.com/device/K120707
Methodology: https://510kreport.com/methodology