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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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