Unisensor AG
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) | K062222 | UNITIP HIGH RESOLUTION CATHETER | FFX | 2007-03-15 | View |
| 510(k) | K003580 | UNITIP GASTROINTESTINAL PRESSURE SENSOR CATHETER | FFX | 2001-07-31 | View |
No matching devices.
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