Last synced on 20 June 2025 at 11:06 pm

Venus BlissMAX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213308
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2022
Days to Decision
100 days
Submission Type
Summary

Venus BlissMAX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213308
510(k) Type
Traditional
Applicant
Venus Concept USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/2022
Days to Decision
100 days
Submission Type
Summary