FDA 510(k) Applications for Medical Device Product Code "KPK"
(Marker, Ostia, Aorto-Saphenous Vein)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K971966 | MED-EDGE, INC. | CORONARY VEIN GRAFT TAG MARKER | 01/26/1998 |
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