510(k) K223516

Device
VX1+
Applicant
Volta Medical
510(k) number
K223516
Product code
DQK
Decision
Substantially Equivalent (SESE)
Decision date
2023-01-21
Date received
2022-11-22
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
No

Applicant Contact#

Contact
Paola Milpied
Address
65 Ave. Jules Cantini Marseille FR 13006 13006

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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