510(k) K013946 ยท NEY System, Ablation, Microwave And Accessories
FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM
| Applicant | Afx, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Feb 27, 2002 |
| Received | Nov 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013946
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.