FDA 510(k) Applications Submitted by Jimin Han

FDA 510(k) Number Submission Date Device Name Applicant
K212253 07/19/2021 Apollo Duet (Model : APD-4000) Weero Co.
K223930 12/30/2022 A1417MCW/A1717MCW/F1417MCW H&abyz Co., Ltd.


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