FDA 510(k) Applications Submitted by JAMES M SHY
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030062 |
01/07/2003 |
ADMIRAL .035 DILATATION CATHETER, MODELS ADL0720-80,ADL0720-135,ADL0820-80, ADL0820-135,ADL0920-80,ADL0920-135,ADL1020-0 |
AVANTEC VASCULAR CORP. |
K030638 |
02/28/2003 |
DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML |
AVANTEC VASCULAR CORP. |
K032436 |
08/07/2003 |
DURAMAX .018 BILIARY STENT SYSTEM |
AVANTEC VASCULAR CORP. |
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