FDA 510(k) Applications for Medical Device Product Code "FKO"
(Catheter, Peritoneal Dialysis, Single Use)

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


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