FDA 510(k) Applications Submitted by TECHDEVICE CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110241 | 01/27/2011 | ENDOLOGIX GUIDEWIRE | TECHDEVICE CORPORATION |
| K051137 | 05/04/2005 | TECHDEVICE OCCLUSION BALLOON CATHETER | TECHDEVICE CORPORATION |
| K053028 | 10/27/2005 | TECHDEVICE GUIDEWIRE | TECHDEVICE CORPORATION |
| K053251 | 11/21/2005 | TECHDEVICE GUIDEWIRE | TECHDEVICE CORPORATION |
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