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U.S. Department of Health and Human Services

510(k) Premarket Notification

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31 to 40 of 490 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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510(K)
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nutricath EXCO, INC. K813374 03/15/1982
deseret intracath intravenous catheter WARNER-LAMBERT CO. K821372 06/02/1982
deseret subclavian jugular catheter set WARNER-LAMBERT CO. K821371 06/02/1982
deseret angio guide WARNER-LAMBERT CO. K821577 06/16/1982
deseret subclavian jugular catheter set WARNER-LAMBERT CO. K821699 06/24/1982
leonard/norton hyperalimentation cathet. NORTON PERFORMANCE PLASTICS CORP. K821679 07/02/1982
subclavian DNA MEDICAL, INC. K821929 07/08/1982
deseret subclavian jugular cath. set WARNER-LAMBERT CO. K822023 07/28/1982
intravenous catheter placement unit & ACCESS DEVICES, INC. K823017 11/01/1982
teflon cannula CARDIAC PACEMAKERS, INC. K822776 11/03/1982
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