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KNZ — Accessories, A-V Shunt Class II

FDA Device Classification

Classification Details

Product Code
KNZ
Device Class
Class II
Regulation Number
876.5540
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K842039argon medicalARGON DUAL LUMEN HEMODIALYSIS, CATHETERJanuary 29, 1985
K844612packaging technologiesACUTE HEMODIALYSIS TRAYSDecember 17, 1984
K842864vas-cath of canadaVACCESS FEMORAL CANNULAAugust 8, 1984
K842416medical componentsDUO FLOW CATHETER-MC 54July 26, 1984
K841530medical componentsDOUBLE LUMEN SUBLCAVIAN-FEMORALJune 25, 1984
K841119top surgical manufacturersTOPS DISPOS. INFUSION SET/HEMODIALYSISApril 20, 1984
K840424quintonHEMOCATH REPAIR KITMarch 5, 1984
K840437renal systemsHEMASITE ACCESSORIES MODIFICATIONFebruary 21, 1984
K834510renal systemsRENAFLO AVF SET FOR HEMODIALYSISFebruary 4, 1984
K833139intermedACUTE HEMODIALYSIS TRAYSDecember 22, 1983