# K252569: Carrier XL Delivery Catheter

- Pathway: 510(k) (Special)
- Applicant: Balt USA, LLC
- Decided: Oct 22, 2025 after 69 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- 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 K960806 (1996). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230609: NG Delivery Catheter, Balt USA, LLC (2023) Summary page 5.

## Indications for use
The Carrier XL Delivery Catheter is intended for general intravascular use, including the peripheral, coronary and neuro vasculature for the infusion of diagnostic agents, such as contrast media, and to assist in the delivery of interventional devices, such as distal access catheters, in the neurovasculature.

Source page: https://510kreport.com/device/K252569
Methodology: https://510kreport.com/methodology