510(k) K002992 ยท IKT Electrode, Needle, Diagnostic Electromyograph
DISPOSABLE HYPODERMIC NEEDLE ELECTRODE, MODEL 9013S0421,9013S0431,9013S0441,9013S0451,9013S0461,1013S0421,103S0431
| Applicant | Medtronic Functional Diagnostics A/S, Skovlunde, DK |
| Decision | Substantially Equivalent, Aug 15, 2001 |
| Received | Sep 25, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002992
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.