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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