510(k) K063753 ยท GXD Generator, Lesion, Radiofrequency
GFX NERVE ABLATION SYSTEM
| Applicant | Aci, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Jun 20, 2007 |
| Received | Dec 19, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063753
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.