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CUTERA PICOSECOND LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133945
510(k) Type
Traditional
Applicant
CUTERA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/2014
Days to Decision
231 days
Submission Type
Summary

CUTERA PICOSECOND LASER SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133945
510(k) Type
Traditional
Applicant
CUTERA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/2014
Days to Decision
231 days
Submission Type
Summary