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FDA 510(k) Applications Submitted by Cascination AG
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220300
02/02/2022
OTOPLAN
Cascination AG
K203486
11/27/2020
Otoplan
CAScination AG
K152473
08/31/2015
CAS-One IR
CAScination AG
K143024
10/21/2014
CAS-One Liver
CAScination AG
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