FDA 510(k) Applications for Medical Device Product Code "NHW"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K024071 | GUIDANT CORPORATION, CARDIAC SURGERY | GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM | 02/14/2003 |
K020701 | GUIDANT CORPORATION, CARDIAC SURGERY | SYNCRUS INTERNAL CARDIOVERSION SYSTEM | 05/24/2002 |