510(k) K810206 ยท GXY Electrode, Cutaneous
DUAL TYPE ELECTRODE
| Applicant | Professional Instruments Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 20, 1981 |
| Received | Jan 26, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810206
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.