Afx, Inc. · Class II · Cleared Feb 27, 2002
| K-number | K013946 |
| Device name | FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM |
| Applicant | Afx, Inc. |
| Product code | NEY |
| Device class | Class II |
| Decision date | Feb 27, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov