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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