Neuro-Diagnostic Assoc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980866 | MEDI-DX 7000 CPT WITH AMREX ELECTRODES | GWF | 1998-05-20 | View |
| 510(k) | K964622 | MEDI-DX 7000 | LLN | 1997-12-01 | View |
No matching devices.
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