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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