K-number	K190972
Device name	Ambu aScope 4 RhinoLaryngo Intervention
Applicant	Ambu A/S
Product code	EOB
Device class	Class II
Decision date	Jul 12, 2019
Decision	Substantially Equivalent
Regulation	874.4760

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Source

View the full FDA submission: accessdata.fda.gov

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Ambu aScope 4 RhinoLaryngo Intervention

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