510(k) K862028 ยท GXY Electrode, Cutaneous
ULTRAHESIVE II POSTOP ELECTRODE
| Applicant | Medical Devices, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Aug 1, 1986 |
| Received | May 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862028
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.