510(k) K242033

Device
Access25™ Delivery Microcatheter
Applicant
Penumbra, Inc.
510(k) number
K242033
Product code
QJP
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-11
Date received
2024-07-11
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
Akshay Kulkarni
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

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