Endotek Corp.
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) | K842124 | EMG MODULE, EMG1, W/OPTIONAL SPEAKER | FAP | 1984-08-08 | View |
| 510(k) | K802374 | ROBERTSON OBTURATION MONITOR INSUFFLA | FAP | 1980-11-24 | View |
No matching devices.
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