# K234074: Next Generation Access Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Balt USA, LLC
- Decided: Jul 2, 2024 after 193 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: 8 generations back to K010954 (2001). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221822: BENCHMARK BMX81 Access System, Penumbra, Inc. (2022) Summary page 4.

## Most influential descendants
- K254223: Next Generation 088 Catheter (2026), 0 descendants of its own

## Indications for use
The Next Generation Access Catheter is indicated for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.

Source page: https://510kreport.com/device/K234074
Methodology: https://510kreport.com/methodology