510(k) K173815 ยท IKT Electrode, Needle, Diagnostic Electromyograph
Allergan Botox Needle Electrode
| Applicant | Natus Manufacturing Limited, Gort, IE |
| Decision | Substantially Equivalent, Jun 29, 2018 |
| Received | Dec 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173815
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.