510(k) K062792 ยท EGJ Device, Iontophoresis, Other Uses
ERCHONIA IOTO_240
| Applicant | Erchonia Medical, Inc., Littleton CO, US |
| Decision | Substantially Equivalent, Mar 1, 2007 |
| Received | Sep 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062792
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.