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AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003978
510(k) Type
Traditional
Applicant
AFX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2001
Days to Decision
151 days
Submission Type
Summary

AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003978
510(k) Type
Traditional
Applicant
AFX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2001
Days to Decision
151 days
Submission Type
Summary