Somnitec, 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) | K911989 | GOLD CUP EEG CUTANEOUS ELECTRODE W/LEAD AND EXT. | GXY | 1991-07-30 | View |
| 510(k) | K912817 | SOMNIMIC (R) | LEL | 1991-07-26 | View |
| 510(k) | K912234 | SOMNIPROBE(R) MODEL NUMBER 10093, MODIFICATION | BZG | 1991-07-22 | View |
| 510(k) | K911990 | ECG FEMALE-TO-PIN SNAP ELECTRODE W/LEADS AND EXT. | DRX | 1991-06-21 | View |
No matching devices.
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