510(k) K083350 ยท GXY Electrode, Cutaneous
TENS/NMES/FES STIMULATING ELECTRODE
| Applicant | Covidien LP, Mansfield MA, US |
| Decision | Substantially Equivalent, Apr 21, 2009 |
| Received | Nov 13, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083350
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.