FDA 510(k) Applications Submitted by ANALOGIC CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K140126 01/16/2014 SONIC WINDOW ANALOGIC CORPORATION
K070829 03/26/2007 SYNEPIX 4600 DETECTOR ANALOGIC CORPORATION
K051903 07/13/2005 FETALGARD LITE-NIBP, MODEL FGL-NIBP ANALOGIC CORPORATION
K172058 07/06/2017 CT6485, CT12885 Analogic Corporation
K182147 08/08/2018 CTXX85 Analogic Corporation
K201231 05/07/2020 CTxx85 CT Scanner Analogic Corporation
K161342 05/13/2016 Sonic Window ANALOGIC CORPORATION


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