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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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