Neurodiagnostics, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K843253 | EMG/NCV & EVOKED RESPONSE, DESIGN W/ | GWF | 1984-11-20 | View |
| 510(k) | K830191 | NEURO DIAGNOSTICS MODEL FCR | GWK | 1983-02-18 | View |
| 510(k) | K801671 | ESG-1 (EVOKED RESPONSE STIMULUS GENER) | GWE | 1980-08-04 | View |
| 510(k) | K801670 | NDI-IKE EMG | GWK | 1980-08-04 | View |
No matching devices.
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