510(k) K251518

Device
Volta AF-Xplorer II
Applicant
Volta Medical
510(k) number
K251518
Product code
DQK
Decision
Substantially Equivalent (SESE)
Decision date
2025-09-12
Date received
2025-05-16
Regulation
870.1425
Classification name
Computer, Diagnostic, Programmable
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
Paola Milpied
Address
65 Ave. Jules Cantini Tour Mediterranee Marseille FR 13006 13006

FDA Registration Numbers

Source Documents

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

Related GUDID Devices

Primary DIBrandCompanyPublished
03770019196069Volta AF-Xplorer IISUBSTRATE HD2025-11-18

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