K-number	K203749
Device name	Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable
Applicant	Ambu A/S
Product code	CBI
Device class	Class II
Decision date	May 3, 2021
Decision	Substantially Equivalent
Regulation	868.5740

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Source

View the full FDA submission: accessdata.fda.gov

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Ambu VivaSight 2 DLT, Ambu VivaSight 2 Adapter Cable

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