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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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