510(k) K081729 ยท GXD Generator, Lesion, Radiofrequency
MODIFICATION TO GFX NERVE ABLATION SYSTEM
| Applicant | Bioform Medical, Inc., Franksville WI, US |
| Decision | Substantially Equivalent, Aug 7, 2008 |
| Received | Jun 18, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081729
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.