510(k) K030800 ยท GXY Electrode, Cutaneous
ELECTROMED REUSABLE NEUROSTIMULATION ELECTRODES
| Applicant | Eletromed, Inc., Betheda MD, US |
| Decision | Substantially Equivalent, Jun 11, 2003 |
| Received | Mar 13, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030800
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.