510(k) K001869 ยท IKT Electrode, Needle, Diagnostic Electromyograph
DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE
| Applicant | Medicotest A/S, Washington DC, US |
| Decision | Substantially Equivalent, Sep 18, 2000 |
| Received | Jun 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001869
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.