510(k) K020907 ยท IKT Electrode, Needle, Diagnostic Electromyograph
NEUROLINE, SUBDERMAL NEEDLE ELECTRODES
| Applicant | Medicotest A/S, Washington DC, US |
| Decision | Substantially Equivalent, Jun 14, 2002 |
| Received | Mar 20, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020907
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.