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Viveve 2.0 System

Page Type
Cleared 510(K)
510(k) Number
K213814
510(k) Type
Traditional
Applicant
Viveve, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2022
Days to Decision
57 days
Submission Type
Summary

Viveve 2.0 System

Page Type
Cleared 510(K)
510(k) Number
K213814
510(k) Type
Traditional
Applicant
Viveve, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2022
Days to Decision
57 days
Submission Type
Summary