510(k) K233201

Device
MIDWAY Delivery Catheter (MIDWAY 43 Delivery Catheter; MIDWAY 62 Delivery Catheter)
Applicant
Penumbra, Inc.
510(k) number
K233201
Product code
QJP
Decision
Substantially Equivalent (SESE)
Decision date
2024-03-27
Date received
2023-09-28
Regulation
870.1250
Classification name
Catheter, Percutaneous, Neurovasculature
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Sheina Rajkumar
Address
One Penumbra Pl. Alameda CA US 94502 94502

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
00815948028197MIDWAYPENUMBRA, INC.2024-04-02
00815948028180MIDWAYPENUMBRA, INC.2024-04-02
00815948028036MIDWAYPENUMBRA, INC.2024-04-02
00815948028029MIDWAYPENUMBRA, INC.2024-04-02

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