Afx, Inc. · Class II · Cleared May 22, 2001
| K-number | K003978 |
| Device name | AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007 |
| Applicant | Afx, Inc. |
| Product code | NEY |
| Device class | Class II |
| Decision date | May 22, 2001 |
| 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