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U.S. Department of Health and Human Services

510(K) Premarket Notification
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Device Name
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510(K)
Number
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Decision
Date
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t-port hp infusion port PFM MEDICAL, INC k071993 10/17/2007
system 1e liquid chemical sterilant processing system STERIS Corporation k102462 09/21/2010
synthetic vinyl patient exam gloves, pre-powdered, yellow BAODING GUANZHONG GLOVE CO., LTD. k062714 12/15/2006
synthes oracle plate SYNTHES SPINE k091159 07/10/2009
synthes (usa) wrist fusion plates (wfp) SYNTHES (USA) k000558 04/14/2000
syngo.via rt image suite Siemens Medical Solutions USA, Inc. k201444 08/13/2020
syngo.ct clinical extensions Siemens Medical Solutions USA, Inc. k173625 03/08/2018
syngo circulation SIEMENS AG, MEDICAL SOLUTIONS k052029 08/09/2005
symmetry iq, model 2000 series, 3000 series HU-FRIEDY MFG. CO., INC k070975 06/21/2007
sydney ivf pvp COOK UROLOGICAL, INC. k031304 03/23/2004

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
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