FDA 510(k) Applications Submitted by Miha Bodytec Gmbh

FDA 510(k) Number Submission Date Device Name Applicant
K221498 05/23/2022 Miha Bodytec II Miha Bodytec GmbH
K201975 07/16/2020 miha bodytec II Miha Bodytec Gmbh
K182519 09/13/2018 Miha Bodytec II Miha Bodytec Gmbh


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