Afx, Inc. is one of 25319 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Afx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM, AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007
2
Total
2
Cleared
0
Denied
Afx, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fremont, US.
Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Afx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Afx, Inc.
2 devices