510(k) K973444 ยท IKT Electrode, Needle, Diagnostic Electromyograph
TECA MYOJECT DISPOSABLE NEEDLE ELECTRODES
| Applicant | Medelec, Inc. D.B.A. Teca Corp., Pleasantville NY, US |
| Decision | Substantially Equivalent, Nov 20, 1997 |
| Received | Sep 11, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973444
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.