FDA 510(k) Applications Submitted by Camilla Wismar

FDA 510(k) Number Submission Date Device Name Applicant
K160766 03/21/2016 Ambu USR, Ambu M AMBU A/S
K181286 05/16/2018 Ambu aScope RLS Slim Ambu A/S
K161656 06/16/2016 Ambu aScope 3 Regular 5.0/2.2, Ambu aScope 3 Slim 3.8/1.2, Ambu aScope 3 Large 5.8/2.8, Ambu aView Monitor AMBU A/S


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