FDA 510(k) Applications Submitted by Lasse Sohrt-Petersen

FDA 510(k) Number Submission Date Device Name Applicant
K233671 11/15/2023 Ambu« aScopeÖ 5 Broncho 4.2/2.2; Ambu« aScopeÖ 5 Broncho 2.7/1.2; Ambu« aViewÖ 2 Advance Ambu A/S


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