510(k) K973529 ยท IKT Electrode, Needle, Diagnostic Electromyograph
NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODES
| Applicant | Medicotest A/S, Washington DC, US |
| Decision | Substantially Equivalent, Nov 20, 1997 |
| Received | Sep 18, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973529
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.