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U.S. Department of Health and Human Services

510(k) Premarket Notification
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111 to 120 of 500 Results *
Decision Date From: 8/1/2003 Decision Date To: 04/23/2024 In Vitro Products: Yes
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510(K)
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xn cal pf Streck K141955 12/05/2014
xn cal Streck K120745 10/19/2012
xn cal Streck K141962 12/05/2014
xn cal Streck K160585 12/22/2016
xl-200 clinical chemistry analyzer, jas glucose reagent, ise reagent pack JAS Diagnostics, Inc. K130915 05/15/2014
xenta drug screen cup, xenta drug screen dipcard Xenta Biomedical Science Co., Ltd. K222955 02/06/2023
xenta drug screen cup, xenta drug screen dipcard Xenta Biomedical Science Co., Ltd. K231137 05/19/2023
x100ht with slide loader with full field peripheral blood smear (pbs) application Scopio Labs Ltd. K220013 05/03/2022
x100 with full field peripheral blood smear (pbs) application Scopio Labs LTD. K201301 10/02/2020
x-cal Streck K083200 02/03/2009

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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