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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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