# K100826: Penumbra Catherer 025

- Pathway: 510(k) (Traditional)
- Applicant: Penumbra, Inc.
- Decided: Jul 13, 2010 after 111 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: 5 generations back to K010954 (2001). 12 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082290: Neuron Delivery Catheter 070, Penumbra, Inc. (2008) Summary page 2.
- K083125: Neuron Select Catheter Size 070, Penumbra, Inc. (2008) Summary page 3.
- K070970: Neuron Support Catheter System, Model 5F/6F, Penumbra, Inc. (2007) Summary page 3.
- K042568: Excelsior 1018 and SL-10 Microcatheters, Boston Scientific Corp (2004) Summary page 3.

## Most influential descendants
- K152840: Lantern Delivery Microcatheter (2015), 1 descendant of its own
- K242033: Access25™ Delivery Microcatheter (2024), 0 descendants of its own

## Indications for use
The Penumbra Catheter 025 is intended to assist in the delivery of diagnostic agents, such as contrast media, and therapeutic agents, such as occlusion coils to the peripheral and neuro vasculature.

Source page: https://510kreport.com/device/K100826
Methodology: https://510kreport.com/methodology