Siegen Corp.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K871964 | SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU. | GWF | 1987-10-01 | View |
| 510(k) | K861884 | NEUROSCOPE SEEG | GWO | 1986-10-14 | View |
| 510(k) | K862430 | SIEGEN HEADPHONES | GWJ | 1986-09-26 | View |
| 510(k) | K844616 | SIEGEN VISUAL STIMULATOR | GWE | 1985-02-14 | View |
| 510(k) | K844646 | SIEGEN SURFACE ELECTRODES | GXY | 1984-12-11 | View |
| 510(k) | K843464 | SIEGEN NEUROSCOPE | GWF | 1984-11-20 | View |
No matching devices.
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