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SYMPHONY RF GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K130689
510(k) Type
Traditional
Applicant
THERMIGEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2013
Days to Decision
247 days
Submission Type
Summary

SYMPHONY RF GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K130689
510(k) Type
Traditional
Applicant
THERMIGEN, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/15/2013
Days to Decision
247 days
Submission Type
Summary