Last synced on 14 November 2025 at 11:06 pm

Venus Versa System

Page Type
Cleared 510(K)
510(k) Number
K152790
510(k) Type
Traditional
Applicant
VENUS CONCEPT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
117 days
Submission Type
Summary

Venus Versa System

Page Type
Cleared 510(K)
510(k) Number
K152790
510(k) Type
Traditional
Applicant
VENUS CONCEPT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
117 days
Submission Type
Summary