# K151082: MicroCross Catheter

- Pathway: 510(k) (Special)
- Applicant: Roxwood Medical, Inc.
- Decided: Jun 7, 2015 after 46 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: 9 generations back to K001992 (2000). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143744: MicroCross Catheter, Roxwood Medical, Inc. (2015) Summary page 4.

## Indications for use
The MicroCross Catheter is intended for use as a conduit for the exchange/support of guidewires in the peripheral and coronary vasculatures. The MicroCross Catheter is also intended to infuse and deliver saline and contrast agents.

Source page: https://510kreport.com/device/K151082
Methodology: https://510kreport.com/methodology