Neuro-Diagnostic Assoc. · Class II · Cleared May 20, 1998
| K-number | K980866 |
| Device name | MEDI-DX 7000 CPT WITH AMREX ELECTRODES |
| Applicant | Neuro-Diagnostic Assoc. |
| Product code | GWF |
| Device class | Class II |
| Decision date | May 20, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 882.1870 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov