510(k) K896874 ยท IKT Electrode, Needle, Diagnostic Electromyograph
DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12
| Applicant | Dantec Medical, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 18, 1990 |
| Received | Dec 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896874
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.