# K242033: Access25™ Delivery Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Penumbra, Inc.
- Decided: Dec 11, 2024 after 153 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 K010954 (2001). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K152840: Lantern Delivery Microcatheter, Penumbra, Inc. (2015) Summary page 5.

## Indications for use
The Access25 Delivery Microcatheter is indicated to assist in the delivery of diagnostic agents, such as contrast media, and therapeutic devices, such as occlusion coils, to the peripheral and neuro vasculature.

Source page: https://510kreport.com/device/K242033
Methodology: https://510kreport.com/methodology