FDA 510(k) Applications Submitted by MINNIE MILDWOFF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071367 | 05/16/2007 | FLEXCEL CAROTID SHUNT (INLYING), MODEL 2020-05 | LEMAITRE VASCULAR, INC. |
| K063467 | 10/24/2006 | SMITH & NEPHEW RF CANNULAE | SMITH & NEPHEW, INC. |
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