FDA 510(k) Applications Submitted by FUJIFILM SonoSite Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K202160 08/03/2020 Sonosite PX Ultrasound System, Sonosite SII Ultrasound System, Sonosite iViz Ultrasound System, Sonosite X-Porte Ultrasound System, Sonosite Edge II Ultrasound System, Sonosite Maxx Ultrasound System FUJIFILM SonoSite Inc.


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