Last synced on 14 November 2025 at 11:06 pm

Vbeam Prima Laser System

Page Type
Cleared 510(K)
510(k) Number
K180593
510(k) Type
Traditional
Applicant
Syneron-Candela
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2018
Days to Decision
91 days
Submission Type
Summary

Vbeam Prima Laser System

Page Type
Cleared 510(K)
510(k) Number
K180593
510(k) Type
Traditional
Applicant
Syneron-Candela
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2018
Days to Decision
91 days
Submission Type
Summary