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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