FDA 510(k) Applications Submitted by SCOTT PAULSON

FDA 510(k) Number Submission Date Device Name Applicant
K130173 01/24/2013 SONOSITE MAXX SERIES ULTRASOUND SYSTEM FUJIFILM SONOSITE,INC.
K160406 02/16/2016 FUJIFILM FC1 Ultrasound System FUJIFILM SonoSite, Inc.
K160674 03/10/2016 Fujifilm Sonosite Vevo MD Imaging System FUJIFILM SONOSITE, INC.
K133134 10/01/2013 X-PORTE ULTRASOUND SYSTEM FUJIFILM SONOSITE,INC.
K113156 10/26/2011 SONOSITE EDGE ULTRASOUND SYSTEM SONOSITE,INC.


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