FDA 510(k) Applications Submitted by AMY WATZKE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K051067 | 04/26/2005 | PRUITT F3 OUTLYING AND INLYING CAROTID SHUNT (WITH AND WITHOUT T-PORT) | LEMAITRE VASCULAR, INC. |
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