# K151896: Houdini Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cruzar Medsystems, Inc.
- Decided: Dec 7, 2015 after 150 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: 7 generations back to K001992 (2000). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083833: Enabler-P Catheter, 1000 Part Number:1160, Endocross, Ltd. (2009) Summary page 4.

## Most influential descendants
- K213466: Houdini Cross Support Catheter (2022), 0 descendants of its own

## Indications for use
The Cruzar Medsystems Houdini 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/K151896
Methodology: https://510kreport.com/methodology