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Cutera enlighten III Laser System

Page Type
Cleared 510(K)
510(k) Number
K160488
510(k) Type
Traditional
Applicant
Cutera, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2016
Days to Decision
249 days
Submission Type
Summary

Cutera enlighten III Laser System

Page Type
Cleared 510(K)
510(k) Number
K160488
510(k) Type
Traditional
Applicant
Cutera, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/28/2016
Days to Decision
249 days
Submission Type
Summary