510(k) K895081 ยท GXY Electrode, Cutaneous
PROMONTORY STIMULATING ELECTRODE
| Applicant | Cadwell Laboratories, Inc., Kennewick WA, US |
| Decision | Substantially Equivalent, Nov 9, 1989 |
| Received | Aug 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895081
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.