510(k) K052878 ยท GXD Generator, Lesion, Radiofrequency
NT-1000
| Applicant | Neuro Therm, Inc., Middleton MA, US |
| Decision | Substantially Equivalent, Jan 23, 2006 |
| Received | Oct 12, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052878
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.