FDA 510(k) Applications for Medical Device Product Code "MAB"
(Marker, Cardiopulmonary Bypass (Vein Marker))
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K052642 | FIRST CALL, INC. | SUTURING WASHER | 01/17/2006 |
| K001915 | T. KOROS SURGICAL INSTRUMENTS CORP. | GRAFT MARKER RING | 04/27/2001 |
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