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Venus Legacy Pro Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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