FDA 510(k) Applications Submitted by Karina Matthiesen

FDA 510(k) Number Submission Date Device Name Applicant
K230428 02/17/2023 Ambu« aScopeÖ 5 Broncho 2.7/1.2, Ambu« aScopeÖ 5 Broncho 4.2/2.2, Ambu« aBoxÖ 2 Ambu A/S
K203749 12/23/2020 Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable Ambu A/S


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