Last synced on 9 May 2025 at 11:05 pm

Venus Versa PRO System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232192
510(k) Type
Special
Applicant
Venus Concept Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2023
Days to Decision
49 days
Submission Type
Summary

Venus Versa PRO System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232192
510(k) Type
Special
Applicant
Venus Concept Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2023
Days to Decision
49 days
Submission Type
Summary