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Venus Legacy Pro Device

Page Type
Cleared 510(K)
510(k) Number
K191528
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2019
Days to Decision
88 days
Submission Type
Summary

Venus Legacy Pro Device

Page Type
Cleared 510(K)
510(k) Number
K191528
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2019
Days to Decision
88 days
Submission Type
Summary