FDA 510(k) Applications Submitted by UNISENSOR AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062222 | 08/02/2006 | UNITIP HIGH RESOLUTION CATHETER | UNISENSOR AG |
| K003580 | 11/20/2000 | UNITIP GASTROINTESTINAL PRESSURE SENSOR CATHETER | UNISENSOR AG |
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