FDA 510(k) Applications Submitted by FUJIFILM New Development U.S.A., Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K170084 01/10/2017 InterLock Trocar FUJIFILM New Development U.S.A., Inc.
K180414 02/15/2018 EPX-4440FN Digital Video Processor with Light Source FUJIFILM New Development U.S.A., Inc.
K162836 10/11/2016 FUJIFILM Surgical System FUJIFILM New Development U.S.A., Inc.


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