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Venus Viva MD Device

Page Type
Cleared 510(K)
510(k) Number
K201164
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2020
Days to Decision
56 days
Submission Type
Summary

Venus Viva MD Device

Page Type
Cleared 510(K)
510(k) Number
K201164
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/2020
Days to Decision
56 days
Submission Type
Summary