# K230609: NG Delivery Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Balt USA, LLC
- Decided: Sep 13, 2023 after 191 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: 6 generations back to K960806 (1996). 8 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K172014: Wedge Microcatheter, MicroVention, Inc. (2018) Summary page 4.

## Most influential descendants
- K252569: Carrier XL Delivery Catheter (2025), 0 descendants of its own

## Indications for use
The NG 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/K230609
Methodology: https://510kreport.com/methodology