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FDA 510(k) Applications Submitted by Reinhold Storch
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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