510(k) K161430 ยท IKT Electrode, Needle, Diagnostic Electromyograph
Myoject Luer Lock Needle Electrode
| Applicant | Natus Manufacturing Limited, Gort, IE |
| Decision | Substantially Equivalent, Mar 2, 2017 |
| Received | May 23, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161430
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.