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

FDA 510(k) Number Submission Date Device Name Applicant
K200714 03/18/2020 AVIEW Coreline Soft Co., Ltd
K192040 07/31/2019 AVIEW Modeler Coreline Soft Co., Ltd
K193220 11/21/2019 AVIEW LCS Coreline Soft Co., Ltd


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