FDA 510(k) Applications Submitted by DFI CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K181024 04/18/2018 DUS 2GP Reagent Strips, DUS 5 Reagent Strips, DUS 10 Reagent Strips DFI Co., Ltd.
K171521 05/24/2017 DUS R-50S (Urine Chemistry system) DFI Co., Ltd.
K102188 08/03/2010 CYBOW READER, MODELS 300 & 720 DFI CO., LTD.


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