FDA 510(k) Applications Submitted by Gurpreet Kaur Rehal

FDA 510(k) Number	Submission Date	Device Name	Applicant
K240848	03/27/2024	Ambu« aScopeÖ 5 Cysto HD (Standard Deflection); Ambu« aScopeÖ 5 Cysto HD (Reverse Deflection); Ambu« aViewÖ 2 Advance	Ambu A/S
K240849	03/27/2024	Ambu« aScopeÖ 5 Cysto HD (Standard Deflection); Ambu« aScopeÖ 5 Cysto HD (Reverse Deflection); Ambu« aBoxÖ 2	Ambu A/S
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