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FDA Product Code

FDA Product Code KNZ — Clearance Directory

Device Class
Class II
21 CFR Citation
876.5540

510(k) Clearances — 10 records

K-Number Device Name Applicant Decision Date Clearance Type Summary
K842039 ARGON DUAL LUMEN HEMODIALYSIS, CATHETER Argon Medical Corp. 1985-01-29 Traditional PDF ↗
K844612 ACUTE HEMODIALYSIS TRAYS Packaging Technologies, Inc. 1984-12-17 Traditional PDF ↗
K842864 VACCESS FEMORAL CANNULA Vas-Cath of Canada , Ltd. 1984-08-08 Traditional PDF ↗
K842416 DUO FLOW CATHETER-MC 54 Medical Components, Inc. 1984-07-26 Traditional PDF ↗
K841530 DOUBLE LUMEN SUBLCAVIAN-FEMORAL Medical Components, Inc. 1984-06-25 Traditional PDF ↗
K841119 TOPS DISPOS. INFUSION SET/HEMODIALYSIS Top Surgical Manufacturers Co. 1984-04-20 Traditional PDF ↗
K840424 HEMOCATH REPAIR KIT Quinton, Inc. 1984-03-05 Traditional PDF ↗
K840437 HEMASITE ACCESSORIES MODIFICATION Renal Systems, Inc. 1984-02-21 Traditional PDF ↗
K834510 RENAFLO AVF SET FOR HEMODIALYSIS Renal Systems, Inc. 1984-02-04 Traditional PDF ↗
K833139 ACUTE HEMODIALYSIS TRAYS Intermed, Inc. 1983-12-22 Traditional PDF ↗

Product code KNZ · Class II · Gastroenterology, Urology. Data: openFDA.