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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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