FDA 510(k) Applications Submitted by FUJIFILM SONOSITE,INC.

FDA 510(k) Number Submission Date Device Name Applicant
K161119 04/20/2016 SonoSite iViz Ultrasound System FUJIFILM SONOSITE,INC.
K152209 08/07/2015 FUJIFILM SonoSite X-Porte Ultrasound System FUJIFILM SONOSITE,INC.
K152983 10/09/2015 FUJIFILM SonoSite iViz Ultrasound System FUJIFILM SONOSITE,INC.
K133454 11/12/2013 SONOSITE EDGE ULTRASOUND SYSTEM FUJIFILM SONOSITE,INC.
K153626 12/18/2015 SonoSite Edge II Ultrasound System FUJIFILM SONOSITE,INC.
K130173 01/24/2013 SONOSITE MAXX SERIES ULTRASOUND SYSTEM FUJIFILM SONOSITE,INC.
K133134 10/01/2013 X-PORTE ULTRASOUND SYSTEM FUJIFILM SONOSITE,INC.


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