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FDA 510(k) Applications Submitted by AFX, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K013946
11/29/2001
FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM
AFX, INC.
K003978
12/22/2000
AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007
AFX, INC.
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