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FDA 510(k) Applications Submitted by ASHITAKA FACTORY OF TERUMO CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170223
01/25/2017
Progreat
ASHITAKA FACTORY OF TERUMO CORPORATION
K161546
06/03/2016
R2P SlenGuide
ASHITAKA FACTORY OF TERUMO CORPORATION
K203521
12/01/2020
FineCross M3
Ashitaka Factory of Terumo Corporation
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