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U.S. Department of Health and Human Services

510(k) Premarket Notification
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71 to 80 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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abl90 flex analyzer RADIOMETER MEDICAL APS K131988 09/17/2013
abl90 flex plus RADIOMETER MEDICAL APS K160153 11/04/2016
abl90 flex series RADIOMETER MEDICAL APS K092686 08/06/2010
abl90 flex, abl90 flex plus Radiometer Medical ApS K170882 04/28/2017
abt glucose control solution AMERICAN BIOLOGICAL TECHNOLOGIES, INC. K083549 12/22/2008
abt glucose control solution level 1,2,3 model, 2120083,2120086, 2120087 AMERICAN BIOLOGICAL TECHNOLOGIES, INC. K091460 08/06/2009
abt glucose control solution, model 2120090 AMERICAN BIOLOGICAL TECHNOLOGIES, INC. K090854 04/16/2009
abt glucose control solution, model: 2120089 AMERICAN BIOLOGICAL TECHNOLOGIES, INC. K090943 05/27/2009
abx erytrol HORIBA ABX K050721 06/01/2005
abx micros crp 200, option im HORIBA ABX K053308 12/29/2005

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