FDA 510(k) Applications for Medical Device Product Code "FKO"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K964514 | CORPAK, INC. | CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS | 06/26/1998 |
K974570 | MEDIGROUP, INC. | PERITONEAL DIALYSIS CATHETER CONNECTOR | 02/27/1998 |