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GENESISPLUS

Page Type
Cleared 510(K)
510(k) Number
K122493
510(k) Type
Traditional
Applicant
CUTERA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2013
Days to Decision
272 days
Submission Type
Summary

GENESISPLUS

Page Type
Cleared 510(K)
510(k) Number
K122493
510(k) Type
Traditional
Applicant
CUTERA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2013
Days to Decision
272 days
Submission Type
Summary