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U.S. Department of Health and Human Services

510(k) Premarket Notification

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41 to 50 of 490 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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510(K)
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central venous catheter PLASMEDICS, INC. K823351 12/09/1982
multi-lumen intravenous catheter MCPHERSON ENTERPRISES, INC. K823565 12/16/1982
intravascular catheter set LAB-A-CATH CORP. K830539 03/17/1983
pre vue TAUT, INC. K830573 03/29/1983
winged catheter ABBOTT LABORATORIES K830765 03/31/1983
i.v. catheter placement unit polyureth CRITIKON COMPANY,LLC K830972 04/27/1983
injection sealing cap 13791 QUINTON, INC. K830541 08/08/1983
deseret subclavian jugular cath-set WARNER-LAMBERT CO. K833091 11/21/1983
deseret angio-guide large vein cath. WARNER-LAMBERT CO. K833092 11/21/1983
intracath intravenous catheter unit PARKE-DAVIS CO. K833135 11/21/1983
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