FDA 510(k) Applications Submitted by ATMOS MedizinTechnik GmbH & Co. KG

FDA 510(k) Number Submission Date Device Name Applicant
K232015 07/06/2023 ATMOS Scope (507.7000.0); ATMOS Scope Pro (507.7050.0); ATMOS Scope iPrime (507.7060.0) ATMOS MedizinTechnik GmbH & Co. KG


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