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FDA 510(k) Applications Submitted by Gurpreet Kaur Rehal
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220606
03/02/2022
Ambu aScope 5 Broncho HD 5.6/2.8, Ambu aScope 5 Broncho HD 5.0/2.2, Ambu aBox 2
Ambu A/S
K210883
03/25/2021
aScope 4 Broncho Regular Sampler Set 5.0/2.2, aScope 4 Broncho Large Sampler Set 5.8/2.8
Ambu A/S
K190972
04/15/2019
Ambu aScope 4 RhinoLaryngo Intervention
Ambu A/S
K191080
04/24/2019
Ambu aScope 4 RhinoLaryngo Slim
Ambu A/S
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