510(k) K120342 ยท IKT Electrode, Needle, Diagnostic Electromyograph
EMG RECORDING ELECTRODE ASSEMBLY
| Applicant | Rhythmlink International, LLC, Columbia SC, US |
| Decision | Substantially Equivalent, Jun 22, 2012 |
| Received | Feb 3, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120342
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.