510(k) K113375 ยท GXY Electrode, Cutaneous
ESWALLOW USA ELECTRODE,ESWALLOW USA LEADWIRE
| Applicant | Eswallow USA, Guntersville AL, US |
| Decision | Substantially Equivalent, Jan 25, 2013 |
| Received | Nov 16, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113375
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.