# K152840: Lantern Delivery Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Penumbra, Inc.
- Decided: Dec 2, 2015 after 64 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: 6 generations back to K010954 (2001). 13 ancestors in all.
1 later device descends 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)
- K100826: Penumbra Catherer 025, Penumbra, Inc. (2010) Summary page 4.

## Most influential descendants
- K242033: Access25™ Delivery Microcatheter (2024), 0 descendants of its own

## Indications for use
Lantern Delivery Microcatheter is intended 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/K152840
Methodology: https://510kreport.com/methodology