K-number	K232582
Device name	Ambu® aScope 5 Broncho 4.2/2.2 Sampler Set
Applicant	Ambu A/S
Product code	EOQ
Device class	Class II
Decision date	Sep 20, 2023
Decision	Substantially Equivalent
Regulation	874.4680

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Source

View the full FDA submission: accessdata.fda.gov

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Ambu® aScope 5 Broncho 4.2/2.2 Sampler Set

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Ambu® aScope 5 Broncho 4.2/2.2 Sampler Set