510(k) K070217 ยท NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE
| Applicant | Neuro Resource Group, Inc., Plano TX, US |
| Decision | Substantially Equivalent, Apr 4, 2008 |
| Received | Jan 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070217
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.