510(k) K010431 ยท GXY Electrode, Cutaneous
LEAD-LOK REUSABLE TENS/ NMES ELECTRODES
| Applicant | Lead-Lok, Inc., Sandpoint ID, US |
| Decision | Substantially Equivalent, Sep 6, 2001 |
| Received | Feb 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010431
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.