510(k) K933807 ยท GXY Electrode, Cutaneous
GROUND PLATE ELECTRODE
| Applicant | Cadwell Laboratories, Inc., Kennewick WA, US |
| Decision | Substantially Equivalent, Jul 26, 1994 |
| Received | Aug 4, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933807
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.