Last synced on 14 November 2025 at 11:06 pm

VX1+

Page Type
Cleared 510(K)
510(k) Number
K223516
510(k) Type
Traditional
Applicant
Volta Medical
Country
France
FDA Decision
Substantially Equivalent
Decision Date
1/21/2023
Days to Decision
60 days
Submission Type
Summary

VX1+

Page Type
Cleared 510(K)
510(k) Number
K223516
510(k) Type
Traditional
Applicant
Volta Medical
Country
France
FDA Decision
Substantially Equivalent
Decision Date
1/21/2023
Days to Decision
60 days
Submission Type
Summary