FDA 510(k) Applications Submitted by Radisen Co., Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K221144 04/20/2022 PEDRA-1417MC, PEDRA-1417MG, PEDRA-1417FC, PEDRA-1417FG Radisen Co., Ltd
K213520 11/03/2021 AXIR-CX Radisen Co., Ltd


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