FDA 510(k) Applications for Medical Device Product Code "DBY"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K013919 | BAYLIS MEDICAL CO., INC. | TORFLEX TRANSSEPTAL GUIDING SHEATH | 02/22/2002 |
K013304 | BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. | BD INTROSYTE PRECISION INTRODUCER, BD INTROSYTE AUTOGAURD SHIELDED INTRODUCER | 01/02/2002 |
K022067 | BOSTON SCIENTIFIC | CONVOY ADVANCED DELIVERY SHEATH | 09/11/2002 |
K013866 | BOSTON SCIENTIFIC | CONVOY ADVANCED DELIVERY SHEATH KIT | 12/14/2001 |
K013282 | W. L. GORE & ASSOCIATES, INC. | GORE INTRODUCER SHEATH | 12/14/2001 |