510(k) K140340 ยท GXY Electrode, Cutaneous
SKINTACT
| Applicant | Leonhard Lang GmbH, Stillwater MN, US |
| Decision | Substantially Equivalent, May 21, 2014 |
| Received | Feb 11, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140340
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.