# K213466: Houdini Cross Support Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cruzar Medsystems, Inc.
- Decided: Oct 20, 2022 after 357 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). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151896: Houdini Catheter, Cruzar Medsystems, Inc. (2015) Summary page 4.

## Indications for use
The Houdini Cross Support Catheter is intended to be used in conjunction with a steerable guidewire to access discrete regions of the peripheral vasculature and for guidewire exchange.

Source page: https://510kreport.com/device/K213466
Methodology: https://510kreport.com/methodology