# K233201: MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)

- Pathway: 510(k) (Traditional)
- Applicant: Penumbra, Inc.
- Decided: Mar 27, 2024 after 181 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 K010954 (2001). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070970: Neuron Support Catheter System, Model 5F/6F, Penumbra, Inc. (2007) Summary page 4.
- K142321: Benchmark Intracranial Access System, Penumbra, Inc. (2015) Summary page 4.

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

Source page: https://510kreport.com/device/K233201
Methodology: https://510kreport.com/methodology