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FDA 510(k) Applications Submitted by Maja Brons
FDA 510(k) Number
Submission Date
Device Name
Applicant
K173727
12/05/2017
Ambu aScope 3 Slim 3.8/1.2 and Ambu aScope 4 Broncho Slim 3.8/1.2; Ambu aScope 3 Regular 5.0/2.2 and Ambu aScope 4 Broncho Regular 5.0/2.2; Ambu aScope 3 Large 5.8/2.8 and Ambu aScope 4 Broncho Large 5.8/2.8; Ambu aView Monitor
Ambu A/S
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