FDA 510(k) Applications Submitted by BRIAN K KEOGH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K031282 | 04/22/2003 | OPTILOCK IMPLANTABLE ACCESS PORT, MODEL 1700-05 | LEMAITRE VASCULAR, INC. |
| K033159 | 09/30/2003 | LEMAITRE VASCULAR STRAIGHT CAROTID SHUNT, MODEL 2002-01, 2002-05, 2003-01, 2003-05, 2004-01, 2004-05, 2005-01, 2005-05 | LEMAITRE VASCULAR, INC. |
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