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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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