510(k) K980866 ยท GWF Stimulator, Electrical, Evoked Response
MEDI-DX 7000 CPT WITH AMREX ELECTRODES
| Applicant | Neuro-Diagnostic Assoc., Laguna Beach CA, US |
| Decision | Substantially Equivalent, May 20, 1998 |
| Received | Feb 19, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980866
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.