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FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K013946
510(k) Type
Traditional
Applicant
AFX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2002
Days to Decision
90 days
Submission Type
Summary

FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K013946
510(k) Type
Traditional
Applicant
AFX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2002
Days to Decision
90 days
Submission Type
Summary