510(k) K881872 ยท GXY Electrode, Cutaneous
TENS ELECTRODE MODEL 238P
| Applicant | Lectec Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jun 16, 1988 |
| Received | May 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881872
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.